U.S. patent application number 15/342475 was filed with the patent office on 2017-02-23 for apparatus for improved breathing.
The applicant listed for this patent is AirWay Technologies, LLC. Invention is credited to Alastair E. McAuley, W. Keith Thornton.
Application Number | 20170049607 15/342475 |
Document ID | / |
Family ID | 46965135 |
Filed Date | 2017-02-23 |
United States Patent
Application |
20170049607 |
Kind Code |
A1 |
Thornton; W. Keith ; et
al. |
February 23, 2017 |
Apparatus for Improved Breathing
Abstract
An apparatus for improved breathing is provided. The apparatus
may include an improved oral appliance, an improved mask, an
improved coupler to couple an oral appliance to a mask, and/or a
combination of these improvements.
Inventors: |
Thornton; W. Keith; (Dallas,
TX) ; McAuley; Alastair E.; (Warkworth, NZ) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
AirWay Technologies, LLC |
Carrollton |
TX |
US |
|
|
Family ID: |
46965135 |
Appl. No.: |
15/342475 |
Filed: |
November 3, 2016 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
14009821 |
Nov 1, 2013 |
|
|
|
PCT/US12/32407 |
Apr 5, 2012 |
|
|
|
15342475 |
|
|
|
|
13080167 |
Apr 5, 2011 |
8662084 |
|
|
14009821 |
|
|
|
|
13080050 |
Apr 5, 2011 |
8671946 |
|
|
13080167 |
|
|
|
|
13080103 |
Apr 5, 2011 |
8783261 |
|
|
13080050 |
|
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61F 5/566 20130101;
A61M 16/06 20130101; A61C 7/08 20130101; A61C 7/36 20130101; A61M
16/0816 20130101 |
International
Class: |
A61F 5/56 20060101
A61F005/56; A61M 16/06 20060101 A61M016/06; A61M 16/08 20060101
A61M016/08 |
Claims
1-118. (canceled)
119. A dental device comprising: a first arch configured to engage
at least some of the teeth of a user's dental arch, the first arch
having a midline that aligns substantially with the anterior
midline of the user's mouth when the first arch is inserted in the
user's mouth; a first coupler coupled to the first arch along the
midline of the arch, a portion of the first coupler configured to
be inside the user's mouth when the first arch is inserted in the
user's mouth; a second arch configured to engage at least some of
the teeth of the user's second dental arch, the second arch having
a midline that aligns substantially with the anterior midline of
the user's mouth when the second arch is inserted in the user's
mouth; a second coupler coupled to the second arch along the
midline of the second arch, the second coupler configured to extend
anterior to the user's second dental arch when the second arch is
inserted in the user's mouth; and a flexible tension element
configured to removably engage the second coupler and the first
coupler, the tension element configured to maintain a forward
position of the first arch relative to the second arch.
120. The dental device of claim 119, wherein the first coupler
comprises: a post coupled to the first arch, the tension element
configured to engage the post; and a cap configured to engage the
post, the cap configured to prevent the tension element from
disengaging from the post when the cap and the tension element are
both engaged with the post.
121. The dental device of claim 119, wherein the second coupler
comprises: a flange coupled to the second arch; a post coupled to
the flange, the tension element configured to engage the post; and
a cap configured to engage the post, the cap configured to prevent
the tension element from disengaging from the post when the cap and
the tension element are both engaged with the post.
122. The dental device of claim 121, wherein the cap is configured
to removably engage the post.
123. The dental device of claim 119, wherein the tension element
defines a first aperture and a second aperture, the first aperture
configured to engage the first coupler, the second aperture
configured to engage the second coupler.
124. The dental device of claim 119, wherein the first arch
comprises: a frame comprising: a left occlusal portion configured
to be positioned proximate at least one of a left bicuspid or a
left molar of the user; a right occlusal portion configured to be
positioned proximate at least one of a right bicuspid or a right
molar of the user, wherein the frame defines an open space between
the left occlusal portion and the right occlusal portion, the space
configured to be positioned proximate an incisor of the user; and a
flange coupled to the left occlusal portion and the right occlusal
portion, the flange extending substantially perpendicular and
mesial to the left and right occlusal portions; and a thermoplastic
moldable tray coupled to the frame.
125. The dental device of claim 124, wherein the thermoplastic
moldable tray extends beyond a lingual edge of the left occlusal
portion in a lingual direction and a lingual edge of the right
occlusal portion in a lingual direction.
126. The dental device of claim 124, wherein the thermoplastic
moldable tray extends beyond a posterior edge of the left occlusal
portion in a posterior direction and a posterior edge of the right
occlusal portion in a posterior direction.
127. The dental device of claim 119, wherein the tension element
allows for lateral movement of the first arch relative to the
second arch when the tension element is engaged with both the first
and second couplers.
128. The dental device of claim 119, wherein the tension element is
configured to exert a tensile force that pulls the first arch
forward relative to the second arch when the tension element is
engaged with both the first and second couplers.
129. A dental device comprising: a first arch configured to engage
at least some of the teeth of a user's dental arch and having a
midline that aligns substantially with the anterior midline of the
user's mouth when the first arch is inserted in the user's mouth; a
first coupler coupled to the first arch along the midline of the
arch; a second arch configured to engage at least some of the teeth
of the user's second dental arch and having a midline that aligns
substantially with the anterior midline of the user's mouth when
the second arch is inserted in the user's mouth; a second coupler
coupled to the second arch; a first tension element configured to
removably engage the second coupler and the first coupler, the
first tension element configured to maintain a forward position of
the first arch relative to the second arch.
130. The dental device of claim 129 further comprising: a third
coupler coupled to the second arch; and a second tension element
configured to removably engage the third coupler and the first
coupler, the second tension element configured to maintain a
forward position of the first arch relative to the second arch.
131. The dental device of claim 130, wherein the second and third
couplers are spaced substantially equidistant from the midline of
the second arch.
132. The dental device of claim 129, wherein the first coupler
comprises: a post coupled to the first arch, the first tension
element configured to engage the post; and a cap configured to
engage the post, the cap configured to prevent the first tension
element from disengaging from the post when the cap and the first
tension element are engaged with the post.
133. The dental device of claim 132, wherein the cap is configured
to removably engage the post.
134. The dental device of claim 129, wherein the first tension
element defines a first aperture and a second aperture, the first
aperture configured to engage the first coupler, the second
aperture configured to engage the second coupler.
135. The dental device of claim 129, wherein the first arch
comprises: a frame comprising: a left occlusal portion configured
to be positioned proximate at least one of a left bicuspid or a
left molar of the user; a right occlusal portion configured to be
positioned proximate at least one of a right bicuspid or a right
molar of the user, wherein the frame defines an open space between
the left occlusal portion and the right occlusal portion, the space
configured to be positioned proximate an incisor of the user; and a
flange coupled to the left occlusal portion and the right occlusal
portion, the flange extending substantially perpendicular and
mesial to the left and right occlusal portions; and a thermoplastic
moldable tray coupled to the frame.
136. The dental device of claim 135, wherein the thermoplastic
moldable tray extends beyond a lingual edge of the left occlusal
portion in a lingual direction and a lingual edge of the right
occlusal portion in a lingual direction.
137. The dental device of claim 135, wherein the thermoplastic
moldable tray extends beyond a posterior edge of the left occlusal
portion in a posterior direction and a posterior edge of the right
occlusal portion in a posterior direction.
138. The dental device of claim 129, wherein the first tension
element allows for lateral movement of the first arch relative to
the second arch when the first tension element is engaged with both
the first and second couplers.
139. The dental device of claim 129, wherein the first tension
element is configured to exert a tensile force that pulls the first
arch forward relative to the second arch when the first tension
element is engaged with both the first and second couplers.
Description
RELATED APPLICATIONS AND CLAIM TO PRIORITY
[0001] This application is a continuation-in-part of U.S. Ser. No.
14/009,821, filed Nov. 1, 2013, which is a U.S. National Stage
Filing under 35 U.S.C. .sctn.371 of International Patent
Application Serial No. PCT/US2012/032407, filed Apr. 5, 2012 and
entitled "Apparatus for Improved Breathing," which is a
continuation of U.S. application Ser. No. 13/080,167, filed Apr. 5,
2011 and entitled "Universal Oral Appliance with a Universal
Coupler," U.S. application Ser. No. 13/080,050, filed Apr. 5, 2011
and entitled "Custom Dental Appliance and Method of Creating a
Custom Dental Appliance," and U.S. application Ser. No. 13/080,103,
filed Apr. 5, 2011 and entitled "Apparatus for Prevention of
Snoring and Improved Breathing." This application claims priority
to each of PCT/US2012/032407 and U.S. application Ser. Nos.
14/009,821, 13/080,167, 13/080,050, and 13/080,103.
TECHNICAL FIELD OF THE INVENTION
[0002] This invention relates generally to medical and dental
devices; and more particularly to an apparatus for improving a
user's breathing.
BACKGROUND
[0003] Many people experience difficulty in sleeping because of
breathing problems. These problems may result in snoring, or the
more serious condition of sleep apnea. One treatment for sleep
breathing disorders involves the use of dental devices for
extending forward the lower jaw of the patient. These devices
operate to more fully open the breathing passageway, thereby
allowing for easier breathing, whether that breathing be through
the nose or through the mouth. Furthermore, many people suffer from
degraded teeth or jaw pain arising from bruxing or the grinding of
teeth during sleep. One treatment for grinding involves the use of
dental devices that put pressure on a patient's front teeth to
relax and unclench the patient's jaw.
[0004] These dental devices may be created in labs after a dentist
sends in a patient's dental impressions. This procedure can cost
the patient substantial time and money because the dentist creates
a dental impression and then the lab creates the dental device
after the dentist sends in the dental impression. Also, these
lab-created dental devices are often designed to target particular
problems. For example, a device for treating snoring may not help a
patient who grinds his teeth.
[0005] People who suffer from sleep problems may seek help from a
sleep laboratory. Doctors at the laboratory may perform tests on
patients as they sleep. Doctors may further test the effectiveness
of various dental devices on the patients as treatment options.
During tests, doctors may need quick access inside a patient's
mouth, and dental devices that hook or attach inside the patient's
mouth may hinder the doctors' ability to gain quick access inside
the mouth. This scenario may also occur during surgery when a
patient is unconscious, and a dental device is inserted into the
mouth to maintain the patient's airway.
[0006] Another treatment for sleep breathing disorders involves the
use of masks to deliver air to users. These masks may also be used
to deliver oxygen or other gases to a user. One difficulty with
these masks is that they often move while the user is sleeping or
they are uncomfortable to the user when worn.
SUMMARY OF THE INVENTION
[0007] In accordance with the teachings of the present invention, a
dental device is provided which may reduce or eliminate
disadvantages and problems associated with prior art devices.
[0008] In one embodiment, a dental device is provided comprising an
arched frame and a moldable tray. The arched frame may be
configured to be positioned proximate to the occlusal surface of a
user's dental arch such that the arched frame extends beyond the
cuspids of the user's dental arch. The arched frame may define a
plurality of apertures and may comprise an adjustment mechanism.
The moldable tray may be coupled to the arched frame and may engage
the plurality of apertures. The moldable tray may comprise a
channel configured to engage at least some of the teeth of the
user's dental arch.
[0009] In a particular embodiment, a dental device is provided
comprising an arched frame, a moldable tray, a second arched frame,
and a second moldable tray. The arched frame may be configured to
be positioned proximate to the occlusal surface of a user's
maxillary arch such that the arched frame extends beyond the
cuspids of the user's maxillary arch. The arched frame may define a
plurality of apertures and may comprise an adjustment mechanism.
The adjustment mechanism may comprise a hook and a threaded
adjustor. The moldable tray may be coupled to the arched frame and
may engage the plurality of apertures. The moldable tray may
comprise a channel configured to engage at least some of the teeth
of the user's maxillary arch. The second arched frame may be
configured to be positioned proximate to the occlusal surface of a
user's mandibular arch such that the second arched frame extends
beyond the cuspids of the user's mandibular arch. The second arched
frame may define a second plurality of apertures and may comprise a
receiving mechanism coupled to the lingual portion of the lower
arched body. The second moldable tray may be coupled to the second
arched frame and may engage the plurality of apertures. The second
moldable tray may comprise a second channel configured to engage at
least some of the teeth of the user's mandibular arch. The hook may
engage the receiving mechanism, and the threaded adjustor may
adjust the forward position of the arched frame relative to the
second arched frame.
[0010] In another embodiment, a dental device may include an arched
frame configured to be positioned proximate to the occlusal surface
of a user's dental arch such that the arched frame extends beyond
the cuspids of the user's dental arch. The arched frame may define
a plurality of apertures. The dental device may further include an
adjustment mechanism coupled to the arched frame. The dental device
may further include a moldable tray coupled to the arched frame.
The moldable tray may engage the plurality of apertures and may
comprise a channel configured to engage at least some of the teeth
of the user's dental arch.
[0011] In another embodiment, a dental device may include an arched
frame configured to be positioned proximate to the occlusal surface
of a user's maxillary arch such that the arched frame extends
beyond the cuspids of the user's maxillary arch. The arched frame
may define a plurality of apertures. The dental device may further
include an adjustment mechanism coupled to the arched frame. The
adjustment mechanism may comprise a hook and a threaded adjustor.
The dental device may further include a moldable tray coupled to
the arched frame. The moldable tray may engage the plurality of
apertures and may comprise a channel configured to engage at least
some of the teeth of the user's maxillary arch. The dental device
may further include a second arched frame configured to be
positioned proximate to the occlusal surface of a user's mandibular
arch such that the arched frame extends beyond the cuspids of the
user's mandibular arch. The second arched frame may define a second
plurality of apertures. The dental device may further include a
receiving mechanism coupled to the lingual portion of the second
arched frame and a second moldable tray coupled to the second
arched frame. The second moldable tray may engage the second
plurality of apertures and may comprise a second channel configured
to engage at least some of the teeth of the user's mandibular arch.
The hook may engage the receiving mechanism and the threaded
adjustor may adjust the forward position of the arched frame
relative to the second arched frame.
[0012] In another embodiment, a universal oral appliance is
provided comprising an arched frame. The arched frame may be
configured to be positioned proximate to the occlusal surface of a
user's dental arch such that the arched frame extends beyond the
cuspids of the user's dental arch when the universal oral appliance
is inserted in the user's mouth. The arched frame may have a
midline that aligns substantially with the anterior midline of the
user's mouth when the universal oral appliance is inserted in the
user's mouth. The arched frame may define a plurality of apertures
and may comprise a universal coupler configured to removably engage
a dental attachment. The universal coupler may comprise a
substantially planar surface proximate to and extending across the
midline of the arched frame. The universal coupler may be
configured to be positioned proximate to the occlusal surface of a
user's incisors when the universal oral appliance is inserted in
the user's mouth. The universal coupler may further comprise a
first rail coupled to a first end of the substantially planar
surface and a second rail coupled to a second end of the
substantially planar surface. The first rail, second rail, and
substantially planar surface may define a slot.
[0013] In another embodiment, a kit for use in constructing a
universal oral appliance is provided. The kit may comprise an
arched frame and a plurality of dental attachments. The arched
frame may be configured to be positioned proximate to the occlusal
surface of a user's dental arch such that the arched frame extends
beyond the cuspids of the user's dental arch when the universal
oral appliance is inserted in the user's mouth. The arched frame
may have a midline that aligns substantially with the anterior
midline of the user's mouth when the universal oral appliance is
inserted in the user's mouth. The arched frame may define a
plurality of apertures and may comprise a universal coupler. The
universal coupler may comprise a substantially planar surface
proximate to and extending across the midline of the arched frame.
The substantially planar surface may be configured to be positioned
proximate to the occlusal surface of a user's incisors when the
universal oral appliance is inserted in the user's mouth. The
universal coupler may further comprise a first rail coupled to a
first end of the substantially planar surface and a second rail
coupled to a second end of the substantially planar surface. The
first rail, second rail, and substantially planar surface may
define a slot. The kit may further comprise a plurality of dental
attachments comprising a rounded projection configured to be the
point of contact between the user's upper and lower dental arches
to prevent the user from clenching his jaw. The plurality of dental
attachments may further comprise a hook configured to engage a
receiving mechanism such that the forward position of a second
arched frame may be adjusted relative to the position of the arched
frame.
[0014] In another embodiment, a universal oral appliance is
provided comprising an arched frame, a moldable tray, and a
plurality of dental attachments. The arched frame may be configured
to be positioned proximate to the occlusal surface of a user's
dental arch such that the arched frame extends beyond the cuspids
of the user's dental arch when the universal oral appliance is
inserted in the user's mouth. The arched frame may have a midline
that aligns substantially with the anterior midline of the user's
mouth when the universal oral appliance is inserted in the user's
mouth. The arched frame may define a plurality of apertures and may
comprise a universal coupler. The universal coupler may comprise a
substantially planar surface proximate to and extending across the
midline of the arched frame. The substantially planar surface may
be configured to be positioned proximate to the occlusal surface of
a user's incisors when the universal oral appliance is inserted in
the user's mouth. The universal coupler may further comprise a
first rail coupled to a first end of the substantially planar
surface and a second rail coupled to a second end of the
substantially planar surface. The first rail, second rail, and
substantially planar surface may define a slot. The moldable tray
may be coupled to the arched frame and may comprise a channel
configured to engage at least some of the teeth of the user's
dental arch. The dental attachment may include a substantially
rounded projection configured to be the point of contact between
the user's upper and lower dental arches to prevent the user from
clenching his jaw. The dental attachment may be an adjustable hook
configured to engage the receiving mechanism such that the forward
position of the arched frame is adjustable relative to the position
of a second arched frame. The dental attachment may be a
handle.
[0015] In another embodiment, a dental device is provided
comprising an arch, a dental attachment with an anchoring element,
a second arch with a second anchoring element, and a tension
element. The arch may be configured to engage at least some of the
teeth of a user's dental arch and may have a midline that aligns
substantially with the anterior midline of the user's mouth when
the arch is inserted in the user's mouth. The dental attachment may
be configured to engage the arch along the midline of the arch. The
dental attachment may comprise an anchoring element configured to
be outside the user's mouth when the arch is inserted in the user's
mouth. The second arch may be configured to engage at least some of
the teeth of a user's second dental arch. The second arch may have
a midline that aligns substantially with the anterior midline of
the user's mouth when the second arch is inserted in the user's
mouth. The second anchoring element may be coupled to the second
arch along the midline of the second arch. The tension element may
be configured to engage the second anchoring element. The tension
element may be further configured to couple to the anchoring
element outside the user's mouth when the arch is inserted in the
user's mouth.
[0016] In another embodiment, a kit for constructing a dental
device is provided. The kit may comprise an arch, a dental
attachment with an anchoring element, a second arch with a second
anchoring element, and a tension element. The arch may be
configured to engage at least some of the teeth of a user's dental
arch and may have a midline that aligns substantially with the
anterior midline of the user's mouth when the arch is inserted in
the user's mouth. The dental attachment may be configured to engage
the arch along the midline of the arch. The dental attachment may
comprise an anchoring element configured to be outside the user's
mouth when the arch is inserted in the user's mouth. The second
arch may be configured to engage at least some of the teeth of a
user's second dental arch. The second arch may have a midline that
aligns substantially with the anterior midline of the user's mouth
when the second arch is inserted in the user's mouth. The second
anchoring element may be coupled to the second arch along the
midline of the second arch. The tension element may be configured
to engage the second anchoring element. The tension element may be
further configured to couple to the anchoring element outside the
user's mouth when the second arch is inserted in the user's
mouth.
[0017] In another embodiment, a dental device is provided
comprising an arched frame, a moldable tray, a dental attachment
with an anchoring element, a second arched frame with a second
anchoring element, a second moldable tray, and a tension element.
The arched frame may be configured to be positioned proximate to
the occlusal surface of a user's maxillary arch such that the
arched frame extends beyond the cuspids of the user's maxillary
arch. The arched frame may define a plurality of apertures. The
moldable tray may be coupled to the arched frame and may engage the
plurality of apertures. The moldable tray may comprise a channel
configured to engage at least some of the teeth of the user's
maxillary arch. The dental attachment may be configured to
removably engage the arch along the midline of the arch. The dental
attachment may comprise an anchoring element configured to be
outside the user's mouth when the arch is inserted in the user's
mouth. The second arched frame may be configured to be positioned
proximate to the occlusal surface of a user's mandibular arch such
that the second arched frame extends beyond the cuspids of the
user's mandibular arch. The second arched frame may define a second
plurality of apertures. The second moldable tray may be coupled to
the second arched frame and may engage the second plurality of
apertures. The second moldable tray may comprise a channel
configured to engage at least some of the teeth of the user's
mandibular arch. The second anchoring element may be coupled to the
second arch along the midline of the second arch. The tension
element may be configured to removably engage the second anchoring
element. The tension element may be configured to couple to the
anchoring element outside the user's mouth when the second arch is
inserted in the user's mouth. The dental attachment may comprise a
post and a buckle coupled to a first end of the post. A second end
of the post may engage the arch. The tension element may comprise a
coupler and a strap coupled to the coupler. The coupler may engage
the second anchoring element. A length of the strap may be
configured to engage the buckle. The buckle may be configured to
substantially secure the length of the strap engaging it. By
increasing the length of the strap engaging the buckle, the forward
position of the arched frame relative to the second arched frame
may be adjusted.
[0018] In another embodiment, a coupler includes a support
structure, at least one flange, and an elongated fastener. The
support structure includes a first channel and a slot passing
through the first channel and being substantially orthogonal to the
first channel. The flange is partially within the first channel and
the flange has a slot disposed through the flange. The elongated
fastener is disposed within the slot of the support structure and
passes through the slot of the flange to engage the flange, such
that the flange is adjustably positioned within the first channel.
The coupler is attached to an oral appliance having an occlusal
surface and to a mask configured to deliver gas to a user, such
that the orientation of the mask to the oral appliance is
adjustable by rotating the flange about the fastener and adjustable
in a direction substantially orthogonal to the occlusal surface of
the oral appliance.
[0019] In another embodiment, an apparatus for use in forming a
dental device includes a substantially rigid arched frame
configured to be positioned proximate to the occlusal surface of a
user's dental arch, such that the arched frame extends beyond the
cuspids of the user's dental arch. The arched frame includes a
first occlusal surface, a second occlusal surface, and a flange.
The first occlusal surface is configured to be positioned proximate
to the occlusal surface of the user's left molars. The second
occlusal surface is configured to be positioned proximate to the
occlusal surface of the user's right molars. The second occlusal
surface is separated from the first occlusal surface. The flange
connects the first and second occlusal surfaces, the flange extends
in a direction substantially orthogonal to the first and second
occlusal surfaces, and the flange is configured to be positioned
labial to the user's dental arch. In another embodiment, a dental
device includes a substantially rigid arched frame and a
thermoplastic material. The substantially rigid arched frame is
configured to be positioned proximate to the occlusal surface of a
user's dental arch, such that the arched frame extends beyond the
cuspids of the user's dental arch. The arched frame includes an
occlusal surface configured to be positioned proximate to the
occlusal surface of the user's dentition. The thermoplastic
material encloses at least a portion of the arched frame, such that
occlusal surface of the arched frame is substantially enclosed by
the thermoplastic material.
[0020] In another embodiment, an improved breathing device includes
a mask, an oral appliance, and a tension element. The mask includes
an opening configured to be positioned in front of the user's mouth
when the mask is positioned on the user's face. The mask further
includes a coupling element proximate to the opening. The oral
appliance includes a maxillary arch with an anchor point proximate
to the midline of the maxillary arch. The tension element is
configured to couple to the a dental device at the anchor point and
to couple to the mask at the coupling element. In certain
embodiments, the tension element may be adjusted to pull the mask
towards the oral appliance. In a particular embodiment, the
coupling element is a strap that extends across a portion of the
opening and includes one or more apertures through which the
tension element may extend, the tension element includes a hook and
a threaded knob, and the anchor point includes a loop, such that
the mask is pulled toward the oral appliance as the threaded knob
is turned while hook is coupled to the loop and extends through an
aperture in the strap.
[0021] In another embodiment, a dental device includes a first
arch, a first coupler, a second arch, a second coupler, and a
flexible tension element. The first arch engages at least some of
the teeth of a user's dental arch. The first arch has a midline
that aligns substantially with the anterior midline of the user's
mouth when the first arch is inserted in the user's mouth. The
first coupler couples to the first arch along the midline of the
arch. The first coupler is inside the user's mouth when the first
arch is inserted in the user's mouth. The second arch engages at
least some of the teeth of the user's second dental arch. The
second arch has a midline that aligns substantially with the
anterior midline of the user's mouth when the second arch is
inserted in the user's mouth. The second coupler couples to the
second arch along the midline of the second arch. The second
coupler extends anterior to the user's second dental arch when the
second arch is inserted in the user's mouth. The flexible tension
element removably engages the second coupler and the first coupler.
The tension element maintains a forward position of the first arch
relative to the second arch. In another embodiment, a dental device
includes a first arch, a first coupler, a second arch, a second
coupler, and a first tension element. The first arch engages at
least some of the teeth of a user's dental arch and has a midline
that aligns substantially with the anterior midline of the user's
mouth when the first arch is inserted in the user's mouth. The
first coupler couples to the first arch along the midline of the
arch. The second arch engages at least some of the teeth of the
user's second dental arch and has a midline that aligns
substantially with the anterior midline of the user's mouth when
the second arch is inserted in the user's mouth. The second coupler
couples to the second arch. The first tension element removably
engages the second coupler and the first coupler. The first tension
element maintains a forward position of the first arch relative to
the second arch.
[0022] Previous dental devices may be constructed in labs
independent of a dentist's office. Labs could not construct custom
dental devices for particular patients without first having the
patients' dental impressions. Labs may also charge patients an
extra fee for constructing the dental devices. In particular
embodiments, the dental device may be constructed at the dentist's
office without sending dental impressions to a lab, thus saving
patients time and money. Furthermore, previous dental devices may
be created to treat only one disorder (such as, for example,
snoring or jaw-clenching). In particular embodiments, the dental
device may be customized to treat multiple dental problems. As an
example, and not by way of limitation, the dental device may
comprise a universal coupler configured to engage various dental
attachments. Each dental attachment may be designed to treat a
different disorder. Additionally, previous dental devices may limit
the lower jaw's range of motion when the dental devices were
inserted in the user's mouth. Previous dental devices may also
limit a third party's access to the user's mouth when the dental
device is in the user's mouth. In particular embodiments, the
dental device may comprise a tension element engaging an anchoring
element outside the user's mouth. The tension element and anchoring
element may pull the user's lower jaw forward without locking the
user's lower jaw in place. Furthermore, a third party may pull on
the tension element to open the user's airway, or a third party may
release the tension element from the anchoring element to quickly
gain access to a user's mouth. Certain embodiments may provide all,
some, or none of these advantages. Certain embodiments may provide
one or more other advantages, one or more of which may be apparent
to those skilled in the art from the figures, descriptions, and
claims included herein.
BRIEF DESCRIPTION OF THE DRAWINGS
[0023] FIG. 1 illustrates an example arched frame.
[0024] FIG. 2A illustrates an example arched frame comprising an
adjustment mechanism.
[0025] FIG. 2B illustrates an example arched frame comprising a
receiving mechanism.
[0026] FIG. 2C illustrates an example arched frame comprising a
receiving mechanism.
[0027] FIG. 3A illustrates an example arched frame comprising an
adjustment mechanism, and an example moldable tray.
[0028] FIG. 3B illustrates an example arched frame comprising a
receiving mechanism, and an example moldable tray.
[0029] FIG. 3C illustrates an example arched frame comprising an
adjustment mechanism, and an example moldable tray.
[0030] FIG. 3D illustrates an example arched frame comprising a
receiving mechanism, and an example moldable tray.
[0031] FIG. 4 illustrates an example dental device in a user's
mouth.
[0032] FIG. 5A illustrates an example universal oral appliance
comprising a universal coupler.
[0033] FIG. 5B illustrates an example universal oral appliance
comprising a universal coupler.
[0034] FIG. 5C illustrates an example universal oral appliance
comprising a universal coupler.
[0035] FIG. 5D illustrates an example universal oral appliance
comprising a universal coupler comprising a guided channel.
[0036] FIG. 5E illustrates an example universal oral appliance
comprising a universal coupler comprising a raised surface.
[0037] FIG. 6 illustrates an example universal oral appliance
comprising a universal coupler, and an example plurality of dental
attachments.
[0038] FIG. 7 illustrates an example dental device in a user's
mouth.
[0039] FIGS. 8A through 8E illustrate an example arched frame.
[0040] FIGS. 9A through 9D illustrate an example moldable tray.
[0041] FIGS. 10A through 10C illustrate an example arched frame
disposed within an example moldable tray.
[0042] FIGS. 10D through 10H illustrate an example dental
device.
[0043] FIGS. 11A and 11B illustrate an example moldable tray and an
example post.
[0044] FIG. 12 illustrates example moldable trays, an example post,
and an example mask.
[0045] FIG. 13 illustrates example moldable trays, an example post,
and an example mask.
[0046] FIG. 14A illustrates an example post.
[0047] FIG. 14B illustrates an example arched frame and tension
element.
[0048] FIGS. 15A and 15B illustrate example flanges.
[0049] FIGS. 16A and 16B illustrate an example post.
[0050] FIGS. 17A through 17F illustrate example flanges engaged
with an example post.
[0051] FIG. 18 illustrates an example post.
[0052] FIGS. 19A and 19B illustrate an example mask.
[0053] FIG. 20 illustrates an example mask, post, and oral
appliance.
[0054] FIG. 21A illustrates an example mask and post.
[0055] FIG. 21B illustrates an example mask, post, and oral
appliance.
[0056] FIG. 22A illustrates an example mask including a strap.
[0057] FIG. 22B illustrates an example tension element, oral
appliance, and mask.
[0058] FIGS. 23A and 23B illustrate an example mask comprising a
strap.
[0059] FIG. 24 illustrates an example tension element, oral
appliance, and mask.
[0060] FIGS. 25A and 25B illustrate an example mask and
adapter.
[0061] FIGS. 26A and 26B illustrate an example adapter.
[0062] FIG. 27 illustrates an example dental device comprising a
universal coupler and an example dental attachment.
[0063] FIG. 28 illustrates an example dental device comprising a
universal coupler and an example dental attachment.
[0064] FIG. 29 illustrates an example arch comprising a dental
attachment.
[0065] FIG. 30 illustrates an example arch comprising a tension
element.
[0066] FIG. 31 illustrates an example dental device comprising a
dental attachment and a tension element.
[0067] FIG. 32 illustrates an example dental attachment and tension
element.
[0068] FIG. 33 illustrates an example dental device in a user's
mouth.
[0069] FIG. 34 illustrates an example process for creating a dental
device.
DETAILED DESCRIPTION OF THE INVENTION
[0070] FIG. 1 illustrates an example arched frame 100. Arched frame
100 may comprise an arched body 105 that defines a plurality of
apertures 110 through arched frame 100. In particular embodiments,
arched frame 100 may be configured to be positioned proximate to
the occlusal surface of a user's dental arch. In some embodiments,
arched frame 100 may extend beyond the cuspids of the user's dental
arch when arched frame 100 is inserted in the user's mouth. In some
embodiments, arched frame 100 may have a consistent thickness
between 1.5 and 2 millimeters. FIG. 2A illustrates an example
arched frame comprising an adjustment mechanism. As shown in FIG.
2A, an arched frame 100 is provided comprising an arched body 105
defining a plurality of apertures 110 and an adjustment mechanism
115. In particular embodiments, arched body 105 may define a
plurality of grooves, or a slot. Adjustment mechanism 115 may be
coupled to arched body 105 along the midline of arched frame 100.
In certain embodiments, Adjustment mechanism 115 may comprise a
hook 120 and a threaded adjustor 125. FIGS. 2B and 2C illustrate
arched frames each comprising a receiving mechanism. As shown in
FIGS. 2B and 2C, an arched frame 100 is provided comprising an
arched body 105 defining a plurality of apertures 110 and a
receiving mechanism 130. In particular embodiments, receiving
mechanism 130 may be a bar spanning a portion of the arch of arched
body 105. In other embodiments, receiving mechanism 130 may be a
surface coupled to the lingual portion of arched frame 100. In some
embodiments, the surface may be rounded.
[0071] In particular embodiments, arched frame 100 may be formed
from any material suitable for dental uses, for example, a hard
plastic. Arched frame 100 may be formed from methyl methacrylate or
a polycarbonate resin thermoplastic such as that sold under the
Registered Trademark Lexan. Such materials are known to those
familiar with dental devices, and other suitable materials may be
used to form arched frame 100 without departing from the intended
scope of the present invention.
[0072] FIGS. 3A and 3C illustrate example arched frames each
comprising an adjustment mechanism and example moldable trays. As
shown in FIGS. 3A and 3C, an arched frame 100 and a moldable tray
135 are provided. Arched frame 100 may comprise an arched body 105
defining a plurality of apertures 110 and an adjustment mechanism
115. Moldable tray 135 may be coupled to arched frame 100 and may
engage the plurality of apertures 110. In particular embodiments,
moldable tray 135 may form through plurality of apertures 110 to
couple to two sides of arched body 105. In some embodiments,
moldable tray 135 may form into a plurality of grooves defined by
arched body 105. In some embodiments, moldable tray 135 may be
secured to arched frame 100 by forming through a slot defined by
arched body 105. Moldable tray 135 may further comprise a channel
140 that is configured to engage at least some of a user's dental
arch. In particular embodiments, channel 140 may engage the
incisors and cuspids of the user's dental arch. In some
embodiments, channel 140 may engage the incisors, cuspids, and some
of the molars of the user's dental arch. In some embodiments,
channel 140 may engage the incisors, cuspids, and all the molars of
the user's dental arch. In particular embodiments, channel 140 may
be shaped to conform to a generic user's teeth. In other
embodiments, channel 140 may be a smooth channel that covers a
user's teeth. In particular embodiments, channel 140 may be further
shaped to conform to a particular user's teeth.
[0073] In particular embodiments, moldable tray 135 may comprise a
polycaprolactone polymer or other aliphatic polyester. One or more
of the polycaprolactone polymers may have the formula:
##STR00001##
where R is an aliphatic hydrocarbon and n may range from
approximately 300 to approximately 650. Certain embodiments may
utilize polycaprolactone polymers using other suitable formulas.
One particular embodiment may utilize Nylon.
[0074] Moldable tray 135 may include any suitable polycaprolactone
polymer or other aliphatic polyester, for example, and not by way
of limitation, the TONE P 700, TONE P 767, or TONE P 787
polycaprolactone polymers manufactured by Union Carbide
Corporation, taken singly or in any combination. A suitable light
cured material, another polymer, or any other suitable material,
such as a filler, coloring agent, stabilizer, antioxidant, or
antimicrobial agent, may be used to replace or combine with one or
more of the polycaprolactone polymers in forming a deformable
material 20 having any number of characteristics, properties, or
uses.
[0075] The TONE polycaprolactone polymers are described in U.S.
Pat. Nos. 5,112,225 and 4,784,123, and in literature distributed by
Union Carbide Corporation, as homopolymers, block copolymers, graft
copolymers, or other polymers that contain epsilon caprolactone.
Polymerization may be initiated using one or more diols, for
example, and not by way of limitation, ethylene glycol; diethylene
glycol; neopentyl glycol; butane diol; hexane diol; or any other
suitable diol.
[0076] In particular embodiments, moldable tray 135 may be custom
molded to a user's teeth. For example, moldable tray 135 may
comprise a material that is moldable when heated. Once heated, the
material may be pressed around a user's dental arch to form a
moldable tray 135 that conforms to the user's teeth. In particular
embodiments, moldable tray 135 may be used with arched frame 100 to
form a custom dental device. For example, arched frame 100 may
comprise a hard plastic material. When moldable tray 135 is forming
around a user's teeth, arched frame 100 may be pressed against
moldable tray 135, so that mold tray 135 forms through plurality of
apertures 110 defined by arched body 105. As moldable tray 135
cools and hardens, moldable tray 135 may couple to arched frame 100
through plurality of apertures 110. In some embodiments, moldable
tray 135 may couple to arched frame 100 through a slot or by
forming into a plurality of grooves. In particular embodiments,
arched frame 100 may provide structural support for moldable tray
135 as moldable tray 135 engages the user's teeth. For example, as
moldable tray 135 engages the user's teeth, arched frame 100 may
prevent moldable tray 135 from deforming or shifting under the
stresses caused by movement of the user's mouth.
[0077] In particular embodiments, a custom dental device may
comprise arched frame 100 and moldable tray 135. A dentist may be
able to construct the custom dental device for a patient without
having to send the patient's dental impressions to a lab. The
dentist may heat moldable tray 135 and press moldable tray 135
around the user's teeth. The dentist may then press arched frame
100 against moldable tray 135 to construct the custom dental
device. As a result, the patient may not have to wait for the lab
to create the dental device, nor does the patient have to pay an
extra fee charged by the lab.
[0078] FIGS. 3B and 3D illustrate example arched frames each
comprising a receiving mechanism, and example moldable trays. As
shown in FIGS. 3B and 3D, an arched frame 100 and a moldable tray
135 are provided. Arched frame 100 may comprise an arched body 105
defining a plurality of apertures 110 and a receiving mechanism
130. Receiving mechanism 130 may be coupled to arched body 105. In
particular embodiments, receiving mechanism 130 may be a bar that
spans a portion of the arch of arched body 105. Moldable tray 135
may comprise a channel 140 that is configured to engage at least
some of the teeth of a user's dental arch.
[0079] FIG. 4 illustrates an example dental device in a user's
mouth. As shown in FIG. 4, a dental device is provided that
comprises an arched frame 100, a moldable tray 135, a second arched
frame 200, and a second moldable tray 235. Arched frame 100 may
comprise an adjustment mechanism 115 that comprises a hook 120 and
a threaded adjustor 125. Moldable tray 135 may be coupled to arched
frame 100. Moldable tray 100 may comprise a channel 140. In some
embodiments, channel 140 may be shaped to conform to a generic
user's maxillary arch 305. In other embodiments, channel 140 may be
a smooth channel that covers some of teeth of a user's maxillary
arch 305. In particular embodiments, channel 140 may be further
shaped to conform to a particular user's maxillary arch 305. Second
arched frame 200 may comprise a second arched body 205 defining a
second plurality of apertures 210. Second arched frame 200 may
further comprise a receiving mechanism 130 coupled to the lingual
portion of second arched body 205. In some embodiments, receiving
mechanism 130 may be a bar that spans a portion of the arch of
second arched body 205. Second moldable tray 235 may be coupled to
second arched frame 200 and may engage second plurality of
apertures 210. Second moldable tray 235 may be configured to engage
some of the teeth of the user's mandibular arch 300. In particular
embodiments, hook 120 may engage receiving mechanism 130. Threaded
adjustor 125 may be used to adjust the forward position of arched
frame 100 relative to second arched frame 200. The relative
positions of the two arched frames 100 and 200 may adjust the
position of the user's maxillary arch 305 relative to the user's
mandibular arch 300. In some embodiments, the relative position of
the user's maxillary and mandibular arches may help to improve a
user's breathing and/or prevent the user from snoring while
sleeping.
[0080] FIGS. 5A and 5B each illustrate an example universal oral
appliance comprising a universal coupler. As shown in FIGS. 5A and
5B, a universal oral appliance is provided comprising an arched
frame 100 and a moldable tray 135 coupled to arched frame 100.
Arched frame 100 may comprise an arched body 105 defining a
plurality of apertures 110. In particular embodiments, arched frame
100 may be configured to be positioned proximate to the occlusal
surface of a user's dental arch such that arched frame 100 extends
beyond the cuspids of the user's dental arch when arched frame 100
is inserted in the user's mouth. Arched frame 100 may have a
midline that aligns substantially with the anterior midline of the
user's mouth when arched frame 100 is inserted in the user's mouth.
Arched frame 100 may further comprise a universal coupler. In
particular embodiments, the universal coupler may comprise a
substantially planar surface 145, a first rail 146, and a second
rail 147. Substantially planar surface 145 may be proximate to and
extend across the midline of arched frame 100. In particular
embodiments, substantially planar surface 145 may be configured to
be positioned proximate to the occlusal surface of a user's
incisors when the universal oral appliance is inserted in the
user's mouth. First rail 146 may be coupled to a first end of
substantially planar surface 145. In particular embodiments, first
rail 146 may be distal to the midline of arched frame 100. In other
embodiments, first rail 146 may be anterior to arched frame 100.
Second rail 147 may be coupled to a second end of substantially
planar surface 145. In particular embodiments, second rail 147 may
be distal to the midline of arched frame 100. In other embodiments,
second rail 147 may be posterior to arched frame 100. First rail
146 and second rail 147 may form an acute angle with substantially
planar surface 145. In particular embodiments, first rail 146,
second rail 147, and substantially planar surface 145 may define a
slot. In particular embodiments, a dental attachment may slide into
the slot and engage arched frame 100. In some embodiments, the
universal coupler may comprise a locking mechanism (such as, for
example, a screw, a tab, or a groove). The screw may secure a
dental attachment to the universal coupler by screwing through the
dental attachment and into the universal coupler. The tab may
secure the dental attachment by engaging the exterior of the dental
attachment or by engaging a slot in the dental attachment. The
groove may secure the dental attachment by frictionally engaging
the dental attachment. In particular embodiments, the universal
coupler may further comprise a stop 148 coupled to substantially
planar surface 145. Stop 148 may be coupled to the labial or
lingual ends of substantially planar surface 145. Alternatively,
stop 148 may be coupled to a distal end of substantially planar
surface 145. Although this disclosure describes a universal oral
appliance comprising arched frame 100, moldable tray 135, and a
universal coupler coupled to arched frame 100, this disclosure
contemplates a one-piece universal oral appliance and a universal
coupler coupled to the universal oral appliance.
[0081] FIG. 5C illustrates an example universal oral appliance
comprising a universal coupler. As shown in FIG. 5C, a universal
oral appliance is provided comprising an arched frame 100 and a
moldable tray 135 coupled to arched frame 100. Arched frame 100 may
comprise a universal coupler comprising a substantially planar
surface 145, a first rail 146, a second rail 147, and a stop 148.
In particular embodiments, each rail 146 and 147 may comprise a
first segment 149 and a second segment 150. First segment 149 may
be coupled at a first end to substantially planar surface 145, and
second segment 150 may be coupled to a second end of first segment
149. In particular embodiments, first segment 149 and second
segment 150 may be substantially perpendicular to each other.
[0082] FIG. 5D illustrates an example universal oral appliance
comprising a universal coupler comprising a guided channel. As
shown in FIG. 5D, a universal oral appliance is provided comprising
an arched frame 100 and a moldable tray 135. Arched frame 100 may
comprise a universal coupler comprising a substantially planar
surface 145, a first rail 146, a second rail 147, and a stop 148.
First rail 146, second rail 147, and substantially planar surface
145 may define a slot. In particular embodiments, the universal
coupler may further comprise a guided channel 151. Guided channel
151 may be configured to guide a dental attachment through the
slot.
[0083] FIG. 5E illustrates an example universal oral appliance
comprising a universal coupler comprising a raised surface 152. As
shown in FIG. 5E, a universal oral appliance is provided comprising
an arched frame 100 and a moldable tray 135. Arched frame 100 may
comprise a universal coupler comprising a substantially planar
surface 145, a first rail 146, a second rail 147, and a stop 148.
First rail 146, second rail 147, and substantially planar surface
145 may define a slot. In particular embodiments, the universal
coupler may further comprise a raised surface 152. Raised surface
152 may be configured to guide a dental attachment through the
slot. In particular embodiments, raised surface 152 may be further
configured to secure or lock the dental attachment.
[0084] FIG. 6 illustrates an example universal oral appliance
comprising a universal coupler, and an example plurality of dental
attachments 400. As shown in FIG. 6, an example universal oral
appliance is provided that comprises an arched frame 100 and a
moldable tray 135. Arched frame 100 comprises an arched body 105
that defines a plurality of apertures 110. Arched frame 100 further
comprises a universal coupler. The universal coupler may comprise a
substantially planar surface 145, a first rail 146, a second rail
147, and a stop 148. In particular embodiments, first rail 146,
second rail 147, and substantially planar surface 145 may define a
slot. FIG. 6 also illustrates a plurality of dental attachments
400. In particular embodiments, the plurality of dental attachments
400 may comprise dental attachments configured to treat different
disorders. For example, the plurality of dental attachments 400 may
include a hook 405, a substantially rounded projection 415, and an
adjustable hook 420. Other attachments may include a handle or any
other appropriate attachment configured for use with an oral
appliance. A user or a medical professional may choose which dental
attachment to use without having to hire a lab to construct a new
oral appliance. In some embodiments, dental attachments 400 may be
configured to engage the slot.
[0085] FIG. 7 illustrates an example dental device in a user's
mouth. As shown in FIG. 7, a dental device is provided that
comprises an arched frame 100, a moldable tray 135 coupled to
arched frame 100, a second arched frame 200, and a second moldable
tray 235 coupled to arched frame 200. Arched frame 100 may comprise
a universal coupler. The universal coupler may comprise a stop 148.
Moldable tray 135 may comprise a channel 140 that is configured to
engage at least some of the teeth of the user's maxillary arch 305.
Second arched frame 200 may comprise a second arched body 205 that
defines a second plurality of apertures 210. Second arched frame
200 may further comprise a receiving mechanism 130 that spans the
lingual portion of second arched frame 200. In particular
embodiments, receiving mechanism 130 may be a bar. Second moldable
tray 235 may engage second plurality of apertures 210. The dental
device further comprises a dental attachment that is configured to
engage the universal coupler. In some embodiments, the dental
attachment may be an adjustable hook 420 that comprises a hook 120
and a threaded adjustor 125. Hook 120 may engage receiving
mechanism 130. Threaded adjustor 125 may be used to adjust the
forward position of second arched frame 200 relative to arched
frame 100. This adjustment may adjust the forward position of the
user's mandibular arch 300 relative to the position of the user's
maxillary arch 305. In some embodiments, this adjustment may help
to prevent the user from snoring while sleeping.
[0086] FIG. 8A illustrates an example arched frame 700. Arched
frame 700 may include an occlusal surface 702 and a flange 706. In
particular embodiments arched frame 700 may be configured to be
positioned proximate to a user's dental arch, with occlusal surface
702 positioned proximate to the occlusal surface of the user's
dental arch. In certain embodiments, occlusal surface 702 may be
contiguous throughout the length of arched frame 700. In
alternative embodiments, as shown in FIG. 8A, occlusal surface 702
may not be contiguous throughout the length of arched frame 700.
For example, occlusal surface 702 may have a first portion
configured to be positioned proximate to the user's left bicuspid
and first molar; and have a second portion configured to be
positioned proximate to the user's right bicuspid and first molar.
As shown in FIG. 8A, in certain embodiments, occlusal surface 702
may not extend to the area proximate to the user's incisors.
Certain embodiments in which the occlusal surface 702 is not
contiguous throughout the length of arched frame 700 may allow for
improved flexibility of arched frame 700. In certain embodiments,
arched frame 700 may be capable of flexing inward and/or outward,
allowing arched frame 700 to conform to a wider variety of dental
arch shapes and sizes. Such embodiments may also improve the
ability of arched frame 700 to accommodate the overlap of the
user's maxillary and mandibular incisors, allowing the user's jaw
to close more fully. In certain embodiments, occlusal surface 702
may have a thickness of approximately 1.5 millimeters, although
other thicknesses may be used.
[0087] Flange 706 may run along the labial edge of arched frame
700. In certain embodiments, flange 706 may be contiguous
throughout the length of arched frame 700. In alternative
embodiments, as shown in FIG. 8A, flange 706 may not be contiguous
throughout the length of the arched frame. For example, flange 706
may include a distal flange portion 708 and a mesial flange portion
710, separated by a flange recess 712. In certain embodiments,
because flange 706 is positioned proximate to the labial surface of
the user's dental arch, it may be pushed outward by the labial
surface of the user's dental arch when arched frame 700 is inserted
into the user's mouth during the molding process, allowing arched
frame 700 to automatically flex and align with the user's dental
arch, which may improve the ability of arched frame 700 to
accommodate different dental arch sizes and shapes. In certain
embodiments, flange recesses 712 may allow for improved flexibility
of arched frame 700. In addition, when arched frame 700 is used
with deformable material, flange recesses 712 may allow the
deformable material to form an improved mold of the user's teeth.
In some embodiments, flange recess 712 may improve the user's
ability to press moldable material against their teeth during the
molding process, which allow for improved dental molds. In certain
embodiments, mesial flange portion 710 may allow for an improved
mold when arched frame 700 is pressed toward the user's teeth
during fitting. As shown in FIG. 8A, in certain embodiments mesial
flange portion 710 may have a thickness greater than that of distal
flange portion 708. For example, mesial flange portion 710 may have
a thickness of approximately 3 millimeters and distal flange
portion 708 may have a thickness of approximately 1.5 millimeters,
although other thicknesses may be used. In such embodiments, the
greater thickness of mesial flange portion 710 may improve the
stability of arched frame 700 during flexion and may provide a more
secure anchor point for other attached structures, such as anterior
structure 716 shown in FIG. 8B.
[0088] FIG. 8B illustrates another example arched frame 700 having
occlusal surface 702, flange 706, and an anterior structure 716. As
shown in FIG. 8B, in certain embodiments occlusal surface 702 may
include an occlusal surface recess 704. When arched frame 700 is
used with deformable material, occlusal surface recess 704 may
allow the deformable material to form a closer mold of the user's
teeth. As shown in FIG. 8B, certain embodiments may include
anterior structure 716 which extends forward from mesial flange
portion 710 in an anterior direction. In certain embodiments,
anterior structure 716 may be fixed to arched frame 700, while in
other embodiments anterior structure 716 may removeably coupled to
arched frame 700. FIGS. 8C and 8D illustrate side views of example
arched frames 700 having occlusal surface 702 and flange 706 with
distal flange portion 708, flange recess 712, and anterior
structure 710.
[0089] FIG. 8E illustrates an isometric view of an example arched
frame 700. As shown in FIG. 8E, arched frame 700 may include
anterior structure 710, occlusal surface 702 that is not contiguous
throughout the length of arched frame 700, and flange 706 that
includes a distal flange portion 708, a flange recess 712, a mesial
flange portion 710, and a mesial flange recess 714. As shown in
FIG. 8E, flange 706 may include mesial flange recess 714 located
approximately at the midline of the arched frame. In such
embodiments, mesial flange recess 714 may allow for improved
conformity with the shape of the user's mouth. In certain
embodiments, the distal ends of arched frame 700 may extend
approximately to the user's first molar when the frame is inserted
into the user's mouth. In alternative embodiments, arched frame 700
may extend to the user's second molar or to the user's third
molar.
[0090] FIGS. 9A through 9D illustrate example moldable trays 730.
As shown in FIG. 9A, moldable tray 730 may include an occlusal
surface 732, an outer rim 734, an inner rim 736, and recesses 738.
Occlusal surface 732 may be configured to be placed proximate to
the occlusal surface of a user's dental arch. Outer rim 734 may be
configured to be positioned proximate to the labial surface of a
user's dental arch. In certain embodiments, inner rim 736 may be
configured to be positioned proximate to the lingual surface of a
user's dental arch. In certain embodiments, inner rim 736 may lie
mostly flat relative to the plane of occlusal surface 732 or may
angle upward slightly. Such embodiments may make moldable tray 730
easier to slide into the user's mouth. In certain embodiments,
inner rim 736 may be capable of being pushed upward or downward to
engage with the lingual surface of the user's dental arch during
the molding process.
[0091] As shown in FIG. 9A, in certain embodiments outer rim 734
may have a thickness greater than that of inner rim 736. For
example, in certain embodiments, outer rim 734 may have a thickness
of approximately 3 millimeters, while inner rim 736 may have a
thickness of approximately 2 millimeters, although these dimensions
are not required. Reduced thickness of inner rim 736 may allow
moldable tray 730 to take up less space in the inner mouth area
behind the teeth, which may allow the user to breath, swallow, and
speak more easily and experience greater comfort. Reduced thickness
of inner rim 736 may also help obviate any need to offer multiple
sizes of moldable tray 730 and arched frame 700. In certain
embodiments, reduced thickness of inner rim 736 may allow other
medical and/or dental devices to be more easily inserted into the
user's mouth. In certain embodiments, as shown in FIG. 9D, inner
rim 736 may be shorter than outer rim 734. A shorter inner rim 736
may allow for easier insertion of moldable tray 730 into the user's
mouth. A shorter inner rim 736 may also reduce the amount of
moldable material in the inner mouth area, which may provide
additional advantages as described above. In certain embodiments,
distal portions of moldable tray 730 may have a reduced height,
which may improve the fit of moldable tray 730 in the user's
mouth.
[0092] As shown in FIG. 9A, in certain embodiments occlusal surface
732 may have one or more recesses 738, which may result from
clamping or otherwise holding in place arched frame 700 during an
overmolding process. In certain embodiments, arched frame 700
illustrated in FIGS. 8A through 8E may have a corresponding recess,
which may allow for improved clamping and alignment during the
manufacturing process.
[0093] FIG. 9B shows another example moldable tray 730 having
occlusal surface 732, outer rim 734, and inner rim 736. As shown in
FIG. 9B, in certain embodiments moldable tray 730 may further
include an anterior structure 740. It should be appreciated that in
certain embodiments the optional anterior structure 740 may be
fixed to moldable tray 730 or it may be removeably coupled to
moldable tray 730.
[0094] In certain embodiments, moldable tray 730 may be composed of
a material that can be heated to a temperature at which the
material softens and becomes capable of being molded to a different
shape. In certain embodiments, the material can be heated in hot
water. In some embodiments, the temperature range at which the
material softens may be approximately 40-80 degrees Celsius,
although materials with other softening ranges may be used. In a
particular embodiment, the target softening temperature may be
approximately 60 degrees Celsius. In certain embodiments, this
material may be a thermoplastic. Such thermoplastic materials may
be heated to a temperature at which the thermoplastic becomes soft
and moldable, at which point it may be molded to the shape of at
least a portion of a user's dental arch and become at least
temporarily fixed in that shape. As one example, moldable tray 730
may comprise a polycaprolactone polymer or other aliphatic
polyester, as discussed above in reference to moldable tray 135. In
particular embodiments, the thermoplastic material may comprise a
cross-linked polycaprolactone reinforced with an aramid fiber such
as the short length aramid fiber sold by Dupont under the brand
name Kevlar.RTM.. In certain embodiments, using polycaprolacton
combined with Kevlar.RTM. may allow moldable tray 730 to soften at
low temperatures and set hard at temperatures of approximately 60
degrees Celsius. In certain embodiments, using polycaprolacton
combined with Kevlar.RTM. may improve the hardness of moldable tray
730 following the molding process, which may improve the ability of
moldable tray 730 to hold its shape when being used to adjust the
user's jaw position and/or hold a mask or other breathing device in
place. In certain embodiments, this increased hardness may also
improve the ability of moldable tray 730 to hold its shape for
longer periods of time. For example, in certain embodiments, this
may allow moldable tray 730 to substantially hold its shape for
periods longer than approximately 1 month, though such period is
not required. Using polycaprolacton combined with Kevlar.RTM. may
also allow for thinner embodiments of moldable tray 730, which may
allow moldable tray 730 to take up less space in the user's mouth.
Examples of polycaprolactone combined with an aramid fiber,
including Kevlar.RTM. and a variety of other fibers, are described
in U.S. application Ser. No. 11/368,991, publication number U.S.
2007/0004993 A1, which is incorporated herein by reference. Such
embodiments may provide an improved moldable material that better
maintains its form when heated, providing increased viscosity which
may prevent the material from flowing excessively around the user's
teeth and/or getting stuck on the user's teeth during the molding
process. Such embodiments may also possess increased strength after
molding. In certain embodiments, the thermoplastic material may be
cross-linked by radiation, which may create cross-linking of
certain molecules to improve the material's shape retention
characteristics and/or make the material better able to return to
its original shape after reheating. In certain embodiments,
radiation may be applied after moldable tray 730 has been
overmolded with arched frame 700, but before being molded to the
user, though this is not required. Cross-linking by radiation is
further described in U.S. Pat. No. 5,415,623, which is incorporated
herein by reference. In certain embodiments, the material may
exhibit slight shrinkage after being molded to the user's dental
arch. In particular embodiments, such shrinkage may be less than
1%. Slight shrinkage of the material following the molding process
may allow for improved fit with the user's dental arch. In some
embodiments, slight shrinkage of the material following the molding
process may allow moldable tray 730 to have a "snap" fit with the
user's dental arch.
[0095] In some embodiments, arched frame 700 may be primarily
composed of a substantially rigid material, such as Nylon or any
other material providing substantial rigidity while allowing
moderate flexion. In certain embodiments, arched frame 700 may be
composed of a material whose form does not substantially changed
when heated to the temperature required to soften the moldable
material of moldable tray 730. For example, in some embodiments,
arched frame 700 may be composed of a material that substantially
maintains its shape when heated up to at least 100 degrees Celsius.
Such materials may include polycarbonate, Nylon, acrylonitrile
butadiene styrene (ABS), or polyethylene. In certain embodiments,
arched frame 700 may be composed of a semi-flexible material, for
example liquid silicone rubber (LSR), approximately having a Shore
30-90 hardness, although this particular hardness is not
required.
[0096] FIGS. 10A through 10C illustrate an example moldable tray
730 substantially surrounding an example arched frame 700. As shown
in FIG. 10A, example moldable tray 730 may include occlusal surface
732, outer rim 734, and inner rim 736; and arched frame 700 may
include occlusal surface 702 and flange 706. As shown in FIG. 10A,
in certain embodiments the labial edge of outer rim 734 may extend
outward beyond the labial edge of flange 706. The lingual edge of
inner rim 736 may also extend inward beyond the labial edge of
occlusal surface 702. As seen in FIG. 10B, in certain embodiments
the distal end of moldable tray 730 may extend distally beyond the
distal end of arched frame 700. In certain embodiments, the distal
end of arched frame 700 may extend approximately to the user's
first molar, while the distal end of moldable tray 730 extends
approximately to the user's second or third molar. In alternative
embodiments, the distal end of arched frame 700 may extend
approximately to the user's second molar, while the distal end of
moldable tray 730 extends approximately to the user's third molar.
In still other embodiments, the distal ends of arched frame 700 and
moldable tray 730 may be approximately coextensive.
[0097] In certain embodiments, when moldable tray 730 is oriented
for placement on, for example, a user's maxillary arch, the
superior surface of outer rim 734 may extend beyond the superior
surface of flange 706 by approximately 2.5 millimeters while the
inferior surface of moldable tray 730 may extend below the inferior
surface of arched frame 700 by approximately 1.5 millimeters,
although these dimensions are not required. In certain embodiments,
moldable tray 730 may extend outward beyond the labial edge of
arched frame 700 by approximately 1.5 millimeters, though other
dimensions are possible. In certain embodiments, moldable tray 730
may extend inward beyond the lingual edge of arched frame 700 by
approximately 1.5 millimeters, though other dimensions are
possible.
[0098] In certain embodiments, flange 706 may help maintain the
shape of outer rim 734. Moldable trays that substantially surround
an arched frame may allow for reduced bulk between a user's
incisors when the tray(s) are inserted into the user's mouth. By
providing moldable trays with less material between the user's
incisors, certain embodiments may allow users to close their mouths
further with the trays inserted, which may improve comfort and/or
effectiveness. Furthermore, moldable trays that substantially
surround arched frame may allow for mouth pieces where only the
moldable material touches the inner surfaces of the user's mouth,
such as the user's gums, lips, and tongue. Such moldable trays may
also allow for improved molding to the user's front teeth. Having
arched frame 700 substantially surrounded by moldable tray 730 may
also reduce the chances of damage to arched frame 700 and may help
hold any broken pieces of arched frame 700 in place, preventing any
such broken pieces from contacting the user's mouth or entering the
user's airway.
[0099] In certain embodiments, arched frame 700 may include
apertures in occlusal surface 702 and/or flange 706, though such
apertures are not required. Such apertures may allow the moldable
material to flow through arched frame 700 during the molding
process, which may provide greater stiffness following the molding
process and may allow for improved alignment of arched frame 700
with moldable tray 730.
[0100] FIGS. 10D through 10G illustrate an example dental device.
The dental device includes a first arch 750, a second arch 755, a
first coupler 760, a second coupler 770, and a flexible tension
element 780. When inserted and/or positioned within a user's mouth,
the dental device maintains a forward position of the user's lower
dental arch relative to the user's upper dental arch. As a result,
the user's breathing may be improved while sleeping.
[0101] First arch 750 includes arched frame 700 and moldable tray
730. First arch 750 may be configured to engage at least some of
the teeth of a user's dental arch, such as for example, the user's
lower dental arch. The midline of first arch 750 may align
substantially with the anterior midline of the user's mouth when
first arch 750 is inserted and/or positioned in the user's mouth.
In some embodiments, moldable tray 730 is coupled to arched frame
700 and is configured to receive the user's teeth. Likewise, second
arch 755 includes arched frame 700 and moldable tray 730.
[0102] Second arch 755 may be configured to engage at least some of
the teeth of a user's dental arch, such as for example, the user's
upper dental arch. The midline of second arch 755 may align
substantially with the anterior midline of the user's mouth when
second arch 755 is inserted and/or positioned in the user's mouth.
In some embodiments, moldable tray 730 is coupled to arched frame
700 and is configured to receive the user's teeth.
[0103] First coupler 760 is coupled to first arch 750. In some
embodiments, first coupler 760 is coupled to first arch 750 along
the midline of first arch 750. First coupler 760 is positioned such
that a portion of first coupler 760 is inside a user's mouth when
first arch 750 is inserted and/or positioned within the user's
mouth. First coupler 760 may engage tension element 780 such that
tension element 780 exerts a tensile force on coupler 760. The
tensile force may pull first arch 750 forward relative to second
arch 755. As a result, a user's jaw may be pulled forward to
improve snoring and/or sleep apnea during sleep. In the embodiments
shown, first coupler 760 includes a post 765 and a cap 785. Cap 785
removably engages post 765. In some embodiments, cap 785 is coupled
to first coupler 760, first arch 750, and/or post 765 by a tether
such that cap 785 does not uncouple from first arch 750 when cap
785 is disengaged from post 765. In this manner, it is more
difficult for a user to lose and/or misplace cap 785. In
alternative embodiments, first coupler 760 is coupled to second
arch 755 and is configured to be within the user's mouth when
second arch 755 is positioned within the user's mouth along the
user's upper dental arch. Tension element 780 engages first coupler
760 to anchor to second arch 755.
[0104] Second coupler 770 is coupled to second arch 755. In some
embodiments, second coupler 770 is coupled to second arch 755 along
the midline of second arch 755. Second coupler 770 is positioned
such that a portion of second coupler 770 extends anterior to a
user's dental arch when second arch 755 is inserted and/or
positioned in the user's mouth. Second coupler 770 engages with
tension element 780 such that tension element 780 anchors to second
coupler 770. Tension element 780 then exerts a tensile force that
pulls first arch 750 forward relative to second arch 755. As a
result, a user's jaw may be pulled forward to improve snoring
and/or sleep apnea during sleep. In some embodiments, a portion of
second coupler 770 extends outside the user's mouth when second
arch 755 is inserted and/or positioned in the user's mouth. Second
coupler 770 includes a flange 773, a post 775, and a cap 790.
Flange 773 extends anterior to the user's dental arch when second
arch 755 is inserted and/or positioned in the user's mouth. In some
embodiments, a portion of flange 773 extends outside of the user's
mouth when second arch 775 is inserted and/or positioned in the
user's mouth. Cap 790 removably engages post 775. In some
embodiments, cap 790 is coupled to second coupler 770, second arch
755, and/or post 775 by a tether such that cap 790 does not
uncouple from second arch 755 when cap 790 is disengaged from post
775. In this manner, it is more difficult for a user to lose and/or
misplace cap 790. In alternative embodiments, second coupler 770 is
coupled to first arch 750 and is configured to extend anterior to
the user's lower dental arch when first arch 750 is positioned in
the user's mouth. Tension element 780 engages second coupler 770 to
exert a tensile force that pull first arch 750 forward relative to
second arch 755.
[0105] Flexible tension element 780 engages first coupler 760 and
second coupler 770 to exert a tensile force on first arch 750 and
second arch 755. In the embodiments shown, flexible tension element
780 removably engages first coupler 760 and second coupler 770 via
post 765 and post 775 respectively to couple first arch 750 to
second arch 755. Flexible tension element 780 may also be referred
to as a strap. Flexible tension element 780 may include elastic or
substantially elastic plastic, rubber, silicone, or any other
material used to form arched frames 700. Flexible tension element
780 defines one or more apertures (e.g. a first aperture and a
second aperture) through which flexible tension element 780 engages
with first coupler 760 and/or second coupler 770 via post 765 and
post 775. When flexible tension element 780 is engaged with post
765 and post 775, caps 785 and 790 may be placed onto posts 765 and
775 to engage posts 765 and 775. In this manner, caps 785 and 790
prevent flexible tension element 780 from disengaging from posts
765 and 775. As a result, flexible tension element 780 couples
first arch 750 to second arch 755 and exert a tensile force that
pulls first arch 750 forward relative to second arch 755. In this
manner, flexible tension element 780 maintains a forward position
of first arch 750 relative to second arch 755.
[0106] In some embodiments, flexible tension element 780 allows for
lateral movement of first arch 750 relative to second arch 755 when
flexible tension element 780 is engaged with both first arch 750
and second arch 755. In this manner, when the dental device is
inserted and/or positioned in the user's mouth, the dental device
may still allow for the user's jaw to move laterally.
[0107] In some embodiments, the length (and/or flexibility or
elasticity) of tension element 780 determines the magnitude of the
tensile force exerted on first arch 750 and second arch 755. For
example, a long tension element 780 may exert less tensile force
than a short tension element 780. This disclosure contemplates the
example dental device and/or the components of the example dental
device including more than one tension element 780 (e.g., as a
kit). Each tension element 780 may have a different length so the
user can adjust the magnitude of the tensile force by selecting a
tension element 780 of a different length. In some embodiments, the
more than one tension element 780 being made using different
materials to adjust the elasticity and/or flexibility of each
tension element. For example, a tension element 780 may be made of
plastic while another tension element 780 is made of rubber. The
two tension elements 780 may exert different tensile forces because
different materials are used to form them. In this manner, the user
can adjust the magnitude of the tensile force by selecting a
tension element 780 of a different material. This disclosure
contemplates the example dental device or the components of the
example dental device being included in a kit that includes
multiple tension elements 780. The lengths of the tension elements
780 may be different. The materials used to form the tension
elements 780 may be different. This disclosure contemplates tension
element 780 being formed from any material (e.g., a semi-rigid
material such as nylon).
[0108] FIG. 10E illustrates the example dental device of FIG. 10D
with first arch 750 coupled to second arch 755. As illustrated in
FIG. 10E, flexible tension element 780 may couple first arch 750 to
second arch 755 by engaging posts 765 and 775 (not shown). Caps 785
and 790 also engage posts 765 and 775 to prevent flexible tension
element 780 from disengaging from posts 765 and 755. Post 765 of
first arch 750 engages flexible tension element 780 through an
aperture from a bottom surface of flexible tension element 780
through a top surface of flexible tension element 780. Post 775 of
second arch 755 engages flexible tension element 780 through an
aperture from the top surface of flexible tension element 780
through the bottom surface of flexible tension element 780.
[0109] FIG. 10F illustrates the example dental device of FIG. 10D
inserted and/or positioned within a user's mouth. As illustrated in
FIG. 10F, first arch 750 is positioned on the user's lower dental
arch and second arch 755 is positioned on the user's upper dental
arch. First arch 750 couples to second arch 755 via flexible
tension element 780. As shown, flange 773 extends anterior to
second arch 755 and out of the user's mouth. Flexible tension
element 780 engages first arch 750 and second arch 755 and caps 785
and 790 prevent flexible tension element 780 from disengaging. In
certain embodiments, cap 785 and the point at which flexible
tension element 780 engages first arch 750 is located within the
user's mouth. Flexible tension element 780 exerts a tensile force
that pulls the first arch 750 forward relative to second arch 755.
As a result, the user's jaw is pulled forward which may improve
breathing when the user is sleeping.
[0110] FIG. 10G illustrates an alternative embodiment of the
example dental device of FIG. 10D. As illustrated in FIG. 10G,
upper arch 755 includes more than one coupler/flange 773. The
couplers may be spaced symmetrically about the midline of second
arch 755. This disclosure contemplates arranging multiple couplers
on any portion of second arch 755 according to a user's needs. Each
coupler couples to the coupler of first arch 750 via a flexible
tension element 780. For example, a first flexible tension element
780 couples a first coupler of second arch 755 to the coupler of
first arch 750. A second flexible tension element 780 couples the
second coupler of second arch 755 to the coupler of first arch 750.
Each flexible tension element 780 is prevented from disengaging the
couplers by caps 790 and cap 785. Each flexible tension element 780
exerts a tensile force that pulls the lower arch 750. The position
of each coupler of second arch 755 may be adjusted to adjust the
direction of the resultant tensile force applied. This disclosure
contemplates second arch 755 and first arch 750 each including any
number of couplers. This disclosure further contemplates
coupler/flange 773 being coupled to lower arch 750 rather than
upper arch 755 and the illustrated coupler of first arch 750 being
instead coupled to second arch 755.
[0111] FIG. 10H illustrates the components of the alternative
embodiment of the example dental device of FIG. 10G. As illustrated
in FIG. 10H, the dental device is similar to the example dental
device of FIG. 10D, except the embodiment of FIG. 10H includes an
additional flange 773 and corresponding post 775 on second arch
755, an additional cap 795, and strap 780 is configured to engage
an additional flange 773 and post 775 of second arch 755. This
disclosure contemplates the dental device including any number of
caps and flanges 773 on any of first arch 750 and/or second arch
755. This disclosure also contemplates flanges 773 being positioned
on any portion of first arch 750 and/or second arch 755. For
example, flanges 773 may be placed symmetrically about a midline of
second arch 755. However, the positions of flanges 773 may be
adjusted and/or changed to adjust the direction of the tensile
force exerted by strap 780 when engaged with first arch 750 and
second arch 755. This disclosure also contemplates strap 780
including defining any number of holes. A user of the dental device
an select which holes to use to engage first and second arches 750
and 755 to adjust the amount of tensile force applied by strap 780.
As a result, the relative forward positions of the arches can be
adjusted by selecting different holes.
[0112] This disclosure contemplates strap 780 comprising two or
more separate straps/tension elements 780. The separate
straps/tension elements 780 may overlap apertures to engage the
same post/flanges 773. This disclosure also contemplates strap 780
comprising two or more straps/tension elements 780 coupled together
in one piece, like the example illustrated in FIG. 10H. Although
strap 780 is one piece, it can be contemplated as a first tension
element 780 coupled to a second tension element 780.
[0113] Although this disclosure describes caps 785, 790, and 795
being separate and distinct from other components of the example
dental devices, this disclosure contemplates one or more of caps
785, 790, and 795 being formed internally with tension element 780.
Furthermore, this disclosure contemplates embodiments that do not
include one or more of caps 785, 790, and 795.
[0114] FIG. 11A illustrates another example moldable tray 730
having occlusal surface 732, outer rim 734, inner rim 736, and
notches 742. In this embodiment, moldable tray 730 is attached to a
post 802 having slot 804, channels 806, and tension element channel
834. FIG. 11B also illustrates a lower isometric view of the same
embodiment showing outer rim 734, notch 742, and a lower surface
744. As shown in FIG. 11A, in certain embodiments moldable tray 730
may be custom molded to fit a particular user's dental arch. In
particular embodiments moldable tray 730 may include one or more
notches 742 which may facilitate grasping the moldable tray for
improved insertion into and removal from the user's mouth. As shown
in FIG. 11B, in certain embodiments lower surface 744 of the
moldable tray 730 may also be molded to fit the user's second
dental arch. In certain embodiments, molding lower surface 744 to
the user's mandibular dental arch may be performed with the user's
mandibular dental arch placed in a particular position relative to
the user's maxillary dental arch. For example, the user's
mandibular dental arch may be extended in the anterior direction,
which may help open a user's airway allowing for improved
breathing. Molding lower surface 744 to the user's mandibular
dental arch may also help hold the user's jaw in a desired
position, such as, for example, when upward force is applied to the
user's mandible by a chin strap or other device.
[0115] In certain embodiments, a second moldable tray configured to
engage with the user's second dental arch may be fused with
moldable tray 730, locating the user's mandibular arch in a
particular position relative to the user's maxillary arch. In such
embodiments, the second moldable tray may be fused to moldable tray
730 prior to forming a mold of the user's dentition. In alternative
embodiments, the second moldable tray may form a separate piece
prior to being molded to the user's dentition. In such embodiments,
the second moldable tray and moldable tray 730 may be heated and
fused together during the molding process.
[0116] Alternative embodiments may utilize a custom-made tray
rather than a moldable tray. In some embodiments, a custom-made
tray may be pre-fitted and then molded from a substantially rigid
material, such as, for example, acrylic. Certain embodiments may
have two separate custom-made trays coupled together via an
adjustment mechanism, such as, for example, those described in U.S.
Pat. No. 7,748,386, which is incorporated herein by reference. In
certain embodiments, such an adjustment mechanism may have wedges
in the side that interact to move the user's lower jaw forward.
[0117] FIG. 12 illustrates two moldable trays 730, a mask 850, and
a coupler 800. FIG. 13 illustrates a side view of the components
shown in FIG. 12. As shown, moldable trays 730 include occlusal
surface 732, outer rim 734, and inner rim 736. Mask 850 is a device
for directing the flow of air and/or other gases to a user. Coupler
800 adjustably couples mask 850 to at least one moldable tray 730.
In the embodiment shown, two moldable trays 730 cooperate to form
an adjustable oral appliance configured to adjustably position the
lower arch of a user relative to the user's upper arch. As shown,
upper moldable tray 730, includes post 802 that extends anterior to
the user's mouth when upper moldable tray 730 is positioned
proximate to the user's maxillary dentition. Similarly, lower
moldable tray 730 includes tension element 830 that extends
anterior to the user's mouth when lower moldable tray 730 is
positioned proximate to the user's mandibular dentition. In this
embodiment, post 802 includes a tension element channel 834 to
receive tension element 830. In certain embodiments, tension
element 830 may be threaded and may be coupled to adjustment knob
832, which may be turned to adjust the position of lower moldable
tray 730 relative to upper moldable tray 730. Although tension
element 830 is described as being threaded, other configurations
may be used to adjust the relative positions of upper and lower
moldable trays 730. In alternative embodiments, tension element 830
may attach to an adjustable oral appliance, such as the oral
appliance described in U.S. Pat. No. 7,748,386. In certain
embodiments, upper moldable tray 730 and lower moldable tray 730
may be used with or without a mask. In these embodiments, moldable
trays 730 may function as an oral appliance only or may be used
during surgery or post-surgery to maintain the user's airway during
the administering of anesthetics or during ventilation, or they may
be in place in the event that resuscitation becomes necessary.
[0118] Mask 850 includes one or more flanges 822, with each flange
822 including a slot 824. Flange 822 may be fixed to or integrally
formed with mask 850; or flange 822 may be removably coupled to
mask 850. However, it should be appreciated that flange 822 may be
fixed to or integrally formed with other mask types, or flange 822
may be removably coupled to and/or interchangeable with other mask
types. In embodiments in which a single flange 822 is used, flange
822 may have a thickness of between 10-22 millimeters, though such
dimensions are not required. In other embodiments, flange 822 may
have a thickness of between 12-18 millimeters. In a particular
embodiment, flange 822 may have a thickness of approximately 14
millimeters. In embodiments having multiple flanges 822, each
flange 822 may have a thickness of between 1-4 millimeters, though
this range is not required. In a particular embodiment having a
multiple flanges 822, one or more of the flanges 822 may have a
thickness of approximately 3 millimeters. In certain embodiments
having multiple flanges 822, when the mask is oriented to the
user's face, the distance between the right edge of the rightmost
flange 822 and the left edge of the leftmost flange 822 may be
similar to the ranges described above for a single flange 822. For
example, in a particular embodiment having two flanges 822, the
span between the inner edges of the flanges may be approximately 6
millimeters and the span between the outer edges of the flanges may
be approximately 14 millimeters, though other dimensions may be
used. Such embodiments may improve the ability of coupler 800 to
prevent deformation outside of the sagittal plane.
[0119] As shown in FIG. 12, mask 850 is a pillow mask with nasal
inserts 852 that may be configured to seal against the user's
nostrils. In certain embodiments, nasal inserts 852 may be fitted
independently to mask 850 and may be capable of rotating
independently to the angle of the user's nostrils. In certain
embodiments, nasal inserts 852 may be removeably coupled to mask
850 and may be interchangeable with different sizes of nasal
inserts 852. In some embodiments, the user may select different
sizes of nasal inserts 852 for each nostril. In alternative
embodiments, nasal inserts 852 may be formed together as a pair and
attached as one unit to mask 850. In other embodiments, nasal
inserts 852 may be fixed permanently to mask 850. In certain
embodiments, mask 850 may have an inlet that is fixed on the top of
the frame for delivering air and/or other gases to mask 850. In
some embodiments, mask 850 may have a ball joint, elbow, or a
combination thereof delivering air and/or other gases to mask 850.
In alternative embodiments, air and/or other gases may be delivered
in the side or the bottom of mask 850. In certain embodiments, air
and/or other gases may be delivered through several different
tubes. In certain embodiments, the user may be able to select one
or more connection points for delivery of air and/or other gases
and plug or otherwise disable other connection points. In other
embodiments, a main hose may attach directly to mask 850 or to an
elbow joint or a ball joint. In certain embodiments, mask 850 may
have a length of flexible tubing that may connect with a main hose.
In certain embodiments, the optional flexible tubing may be
approximately 50-300 millimeters long, though this is not required.
In one example embodiment, mask 850 may have a 250 millimeter-long
flexible tube. In certain embodiments, such tubing may be light,
flexible, and have a smaller diameter than the main hose. In some
embodiments, the flexible tubing may have a diameter of
approximately 12-19 millimeters, while the main hose may have a
diameter of approximately 22 millimeters, though these dimensions
are not required. In one example embodiment, the flexible tubing
may have an internal diameter of approximately 17 millimeters. In
certain embodiments, there may be a connector between the short
flexible tube and the main tube, and in some embodiments this
connector may be capable of swiveling. In particular embodiments,
the connector may be a ball joint or a straight connector. In
certain embodiments, optional headgear may be supplied that
attaches to mask 850, coupler 800, and/or moldable tray 730. Such
headgear may pass along the side of the user's face and may be
capable of holding the main hose or other air-delivery device in a
particular position. For example, in certain embodiments, such
headgear may hold the main hose in place on top of the user's head
or to one or both sides of the user's head. In certain embodiments,
such headgear may also be configured to help hold moldable tray
730, or any other oral appliance, in the user's mouth. In some
embodiments, such headgear may be adjustable at a connection point
on mask 850 and/or at one or more places around the user's head. In
alternative embodiments, the headgear may be formed from a
stretchable material and may require little or no manual
adjustment. In one example embodiment, the headgear may be at least
partially made from Breath-o-prene.RTM., which is a soft,
breathable laminate. In another example embodiment, the headgear
may be at least partially made from silicone or a molded
thermoplastic/fabric composite. In other embodiments, the headgear
may be formed from a combination of these materials, or from a
combination of these and other materials. In certain embodiments, a
chin strap may attach to mask 850, headgear, or moldable tray 730
or any other oral appliance. In some embodiments, mask 850 may have
bias flow (vent holes) to flush out the user's exhaled breath. In
such embodiments, mask 850 may have a plurality of holes to enable
bias flow. In certain embodiments, mask 850 may have approximately
10-50 holes, though this is not required. In one example
embodiment, mask 850 may have approximately 35 holes. In these
embodiments, the holes may be approximately 0.75 millimeters in
diameter, though these dimensions are not required. In certain
embodiments, the holes may have non-uniform cross-sectional shapes
throughout the length of the holes. In one example embodiment, one
or more of the holes may be rounded and have an opening diameter of
approximately 1.2 millimeters, the diameter of the hole falling to
approximately 0.75 millimeters when moving through the hole and
then expanding again to a diameter greater than 0.75 millimeters
when moving through to the other end of the hole. In alternative
embodiments, the holes may be tapered from one side or the other,
or the holes may be straight throughout. In certain embodiments,
having many small holes may slow the flow of gas and may reduce the
draft and noise of such flow. In other embodiments, mask 850 may
have no holes, which may enable closed-loop ventilation. In certain
embodiments, mask 850 may be first formed in two or more distinct
pieces and then joined, for example, by welding, gluing, clipping,
screwing, latching, strapping, or otherwise fixing the pieces
together. In other embodiments, the mask may initially be formed as
a single piece. Furthermore, those skilled in the art will
appreciate that the headgear, tubes, bias holes, chin straps,
attachments, assembly features, and other aspects described above
may also apply to other masks described herein.
[0120] Post 802 may include one or more channels 806 and a slot
804. In the embodiment shown, coupler 800 is formed by two flanges
822 engaging two channels 806. The movement of flanges 822 relative
to channels 806 is limited by fastener 805 in slot 804. Fastener
805 may represent any structure that can restrict the movement of
flanges 822 relative to channels 806. In certain embodiments,
fastener 805 may be a pin, screw, or bolt. In the embodiment shown,
fastener 805 is a threaded hex-head bolt that engages a hex-head
counter sink 807 on one side of post 802 and a tightening knob 808
on the other side of post 802. In certain embodiments, a hex-head
(or other appropriately shaped) countersink may prevent rotation of
fastener 805 while tightening knob 808 or other appropriate
structure is fixing the position of fastener 805. In a particular
embodiment, both sides of post 802 may include a countersink, such
that a user may select to position tightening knob 808 on either
side of post 802. This flexibility may make the use of tightening
knob 808 equally convenient to left-handed and right-handed users.
In alternative embodiments, post 802 may include an additional
tightening knob opposite tightening knob 808, enabling adjustment
from either side of post 802.
[0121] FIG. 14A illustrates the anterior end of an example post 802
and FIG. 14B illustrates an example anterior view of an example
arched frame 700 with a tension element 830. As shown in FIG. 14B,
in certain embodiments at least a portion of the tension element
may be threaded, and the threaded portion may engage with the
tension element adjustor 832. In the embodiments shown, post 802
includes D-shaped slot 834 and tension element 830 has a
corresponding D-shaped cross-section. In certain embodiments, the
D-shaped slot 834 and tension element 830 may substantially prevent
tension element 830 from rotating when adjustment knob 832 is used
to adjust tension element 830. Although a D-shape is illustrated,
other cross-sections may be used to prevent the rotation of tension
element 830 in slot 834. As one example, slot 834 may have a "key"
structure that corresponds with a channel in tension element
830.
[0122] FIGS. 15A and 15B illustrate example flanges 822. As shown
in FIG. 15A, flange 822 may include a slot 824. While FIG. 15B
depicts two distinct flanges 822, alternative embodiments may have
a single flange, multiple flanges, or any other structure which may
be secured in place relative to post 802 by fastener 805. In
alternative embodiments, slot 824 may have various shapes, sizes,
and orientations. In certain embodiments, flanges 822 may be formed
and/or molded as one part. In other embodiments, flanges 822 may be
formed from multiple parts that may be assembled, clipped, screwed,
or overmolded. In various embodiments, flanges 822 may consist of
plastic and/or metal such as stainless steel.
[0123] FIGS. 16A and 16B illustrate an example post 802 having a
fastener 805, channels 806, countersink 807, tightening knob 808,
and a tension element channel 834. As shown in FIG. 16A, an end of
fastener 805 may be configured to engage with countersink 807. In
certain embodiments, as shown in FIG. 16B, at least a portion of
fastener 805 may be threaded. As shown in FIG. 16B, in some
embodiments slot 804 (not shown) may cross laterally through post
802, allowing fastener 805 to pass laterally through post 802
across channels 806. In some embodiments, when flanges 822 are
disposed in channel 806, slots 824 may substantially align with
slot 804, allowing fastener 805 to pass through both slot 804 and
slots 824. In such an embodiment, tightening knob 808 may be
adjusted to increase or decrease lateral force exerted along the
long axis of fastener 808. Adjusting tightening knob 808 in such an
embodiment may operate to secure flanges 822 in place relative to
post 802. In certain embodiments, an attached mask or breathing
device may be moved into the desired position relative to the
user's face and then fixed into that position by adjusting
tightening knob 808.
[0124] In certain embodiments, post 802 may be formed and/or molded
as one part. In other embodiments, post 802 may be formed from
multiple parts that may be assembled, clipped, screwed, or
overmolded. In various embodiments, post 802 may consist of plastic
and/or metal such as stainless steel.
[0125] FIGS. 17A through 17F illustrate various positions of an
example coupler 800. As shown in FIG. 17A, coupler 800 may include
a flange 822 with slot 824 and a post 802 having a fastener 805 and
countersink 807. As shown in FIGS. 17A through 17F, in certain
embodiments, flange 822 may be capable of moving in the
superior-inferior direction relative to post 802, moving in the
anterior-posterior direction relative to post 802, and rotating
around fastener 805. In alternative embodiments, flange 822 may be
capable of moving in the superior-inferior direction relative to
post 802 and rotating around fastener 805. In certain embodiments,
flange 822 may be limited to adjustment, rotation, and/or movement
within the sagittal plane. In some embodiments, post 802 may
include an additional joint that may provide adjustment, rotation,
and/or movement in one or more additional directions. In certain
embodiments, flange 822 may be adjusted vertically approximately
+/-10 mm, though other ranges may be used. For example, other
embodiments may have vertical adjustment ranges of between +/-7 mm
and +/-14 mm. In certain embodiments, flange 822 may be adjusted in
the anterior-posterior direction approximately +/-5 mm, though
other ranges may be used. For example, other embodiments may have
horizontal adjustment ranges of between +/-3 mm and +/-8 mm. In
certain embodiments, when flange 822 has a desired position and
orientation, tightening knob 808 may be adjusted to secure flange
822 in place relative to post 802.
[0126] FIG. 18 illustrates another example post 882 having a
fastener 805, plates 884, channels 806, tightening knob 808, and
plate 886. In particular embodiments, plates 884 may define
channels 806, which are configured to receive flanges 822. As shown
in FIG. 18, post 882 may be cylindrical and hollow. In a particular
embodiment, post 882 may consist of metal, such as stainless steal.
In alternative embodiments, post 882 may have various structures,
shapes, and densities and can be made from a wide variety of rigid
materials. In some embodiments, plate 886 may be attached at the
posterior end of post 882. Plate 886 may be configured to couple to
the front of an oral appliance such as those described, for
example, in U.S. Pat. No. 7,748,386, which is incorporated herein
by reference.
[0127] FIG. 19A illustrates an example mask 890 having flanges 822
with slots 824 and a hose coupler 854 coupled to a hose 870. FIG.
19B illustrates a side view of mask 890, showing opening 856 and
flanges 822. In certain embodiments, as shown in FIG. 19B, flanges
822 may be fixed to or integrally formed with mask 890. In
alternative embodiments, flanges 822 may be removably coupled to
the anterior surface of mask 890. In some embodiments, opening 856
may allow structures, such as post 802 or post 882, to pass through
the front of mask 890 and couple with flanges 824. In certain
embodiments, opening 856 may be sized to accommodate various
positions and orientations of post 802 relative to mask 890.
[0128] FIG. 20 illustrates an example mask 892 coupled to an
example post 802. As shown, mask 892 includes a seal 860, opening
856, flanges 822, and a hose coupler 854. As shown, post 802 is
attached to moldable tray 730 inside the user's mouth, allowing
mask 892 to be adjustably oriented to the user's face. In certain
embodiments, mask 892 may be adjusted vertically, adjusted in the
anterior-posterior direction, and/or rotated in the sagittal plane.
In certain embodiments, as shown in FIG. 20, seal 860 may include
flexible gasket 862 which may be configured to allow post 802 to
pass through it and couple with flanges 824, forming an air-tight
seal around post 802. Flexible gasket 862 may also allow mask 892
to be adjusted to various positions and orientations relative to
the user's face without significantly disturbing post 802 or
breaking the airtight seal of seal 860. In some embodiments, as
shown in FIG. 20, flexible gasket 862 may incorporate or be
surrounded by creases, which may improve the ability of flexible
gasket 862 to accommodate various positions of post 802, though
such creases are not required. In certain embodiments, post 802, or
another suitable post such as post 882, may attach to various oral
appliances, allowing for various combinations of oral appliances,
posts, and masks. In alternative embodiments, flanges 822 may be
contained within a mask, providing the substantially similar
movement and adjustment to mask 892. In such embodiments, fastener
805 may pass through a gasket in the mask's seal to a position
outside the mask where it could be operated by a user.
[0129] Having mask 892 secured to the user's oral appliance may
obviate the need for the user to wear stabilizing headgear. Such
straps may shift accidentally, may be uncomfortable for the user,
may leave marks on the user's face, and may irritate the user's
face and scalp. Furthermore, since having mask 892 secured to the
user's oral appliance may prevent substantial movement of mask 892
relative to the user's face and prevent leakage, these embodiments
may reduce the need to tighten the mask to the user's face, which
may result in reduced pressure on the user's face and reduced
pressure sores. These embodiments may also provide greater mask
stability during sleep for users who exhibit substantial movement
during sleep. It should be appreciated that all such embodiments
and advantages described with respect to mask 892 may also apply to
other mask described herein, such as, for example, masks 850 and/or
894.
[0130] In alternative embodiments, mask 892 may be held in place by
a tension element attached to an oral appliance, with the tension
element pulling mask 892 toward the oral appliance and the user's
face. In certain embodiments, the pull of the tension element may
be adjusted by a screw, tightening knob, or other adjustment
mechanism. Following adjustment, in certain embodiments mask 892
may be secured via a fastener, such as a hook.
[0131] While FIG. 20 shows mask 892 as a full face mask covering
the user's nose and mouth, FIGS. 21A and 21B illustrate an
alternative mask 894 covering the user's mouth and delivering air
and/or other gases to the user's nose via nasal inserts 852. In
certain embodiments, as shown in FIG. 21B, seal 860 may extend
below the user's chin. Masks with portions that extend below a
user's chin may improve the function of the mask by preventing
and/or reducing the occurrence of the user opening their mouth
while using the mask. Still other embodiments incorporating
different types of masks will be apparent to those skilled in the
art. In certain embodiments, when flanges 822 of mask 894 are
disposed in channels 806 of post 802, movement of mask 894 outside
of the sagittal plane is strongly resisted, which may help prevent
mask leakage if a user lays on his or her side, pushing mask 894
laterally against a surface such as a pillow.
[0132] Various types of masks may be used in other embodiments. For
example, certain embodiments may use pillow masks, which seal
against the user's nostrils; nasal masks, which cover the user's
nose; full face masks, which cover both the user's mouth and nose;
hybrid masks, which have one portion covering a user's mouth and
another portion covering the user's nose or sealing against the
user's nostrils; or oral masks, which cover the user's mouth. Such
masks may be used for the delivery of pressurized air, oxygen,
aerosols, gasses, or medication; and the masks may be vented or
non-vented. Masks included in various embodiments may be used for
continuous positive airway pressure treatment (CPAP), auto-CPAP, or
bilevel or closed-loop ventilation; and masks may be custom-fitted
to a particular user or they may be non-custom masks that conform
to different face shapes.
[0133] In certain embodiments, a venting seal may be combined with
the masks and/or oral appliances disclosed herein. In certain
embodiments, the venting seal may be fixed or detachable. The
venting seal may be positioned outside the user's mouth next to the
user's lips or the venting seal may be positioned behind the user's
lips next to the user's teeth. In certain embodiments, the venting
seal may reduce or eliminate the venting of air or other gases from
the user's mouth, such as for example when air or other gases are
being supplied to the user's nose. An example venting seal is
disclosed in U.S. Pat. No. 6,675,802, incorporated herein by
reference. In certain embodiments, the venting seal may be attached
to post 802, post 882, or other appropriate structure, either
removably or permanently.
[0134] FIGS. 22A and 22B and FIG. 23 illustrate an example mask 900
having a hose coupler 902 and a strap 904 with a plurality of
apertures 906. As shown in FIG. 22A, hose coupler 902 may be
configured to attach to a hose 910 which may deliver air and/or
other gases to mask 900. In certain embodiments, as shown in FIG.
23A, strap 904 may span the opening of hose coupler 902. As shown
in FIG. 23A, strap 904 may have a plurality of apertures along its
length. In certain embodiments, as shown in FIG. 22B, a tension
element 920 may pass through one of the plurality of apertures 906
and attach to oral appliance 930, which may be any mouthpiece
configured to couple to tension element 920. FIG. 24 illustrates an
example oral appliance 930, mask 900, and tension element 920. As
shown in FIG. 24, tension element 920 has a threaded knob 924 and a
hook 922. Oral appliance 930 includes a receiver to engage tension
element 920 to pull mask 900 towards oral appliance 930. In certain
embodiments, the receiver in oral appliance 930 may be a loop, a
latch, or a slot. In a particular embodiment, tension element 920
includes hook 922 and threaded knob 924. In alternative
embodiments, tension element 920 may include one or more
alternative structures to pull mask 900 towards oral appliance
930.
[0135] FIGS. 25A and 25B illustrate an example mask 950 and adapter
960. As shown in FIGS. 26A and 26B, in certain embodiments adapter
960 may include a hose coupler 962, a strap 904 having a plurality
of apertures 906, and a mask coupler 968. In some embodiments, hose
coupler 902 may be configured to couple with a hose 910. As shown
in FIGS. 25A and 25B, mask coupler 968 may be configured to couple
with hose coupler 952 of mask 950, allowing adapter 960 to couple
with mask 950. When adapter 960 is coupled to mask 950, adapter 960
may allow mask 950 to interact with hose 910 and tension element
920 as described in the above description of mask 900.
[0136] FIG. 27 illustrates an example dental device comprising a
universal coupler and an example dental attachment. As shown in
FIG. 27, a dental device is provided comprising an arched frame
100, a moldable tray 135, a second arched frame 200, and a second
moldable tray 235. Arched frame 100 may comprise a universal
coupler comprising a substantially planar surface 145. In
particular embodiments, a hook 405 may be configured to engage the
universal coupler. In particular embodiments, second arched frame
200 may comprise a receiving mechanism 130 coupled to the lingual
portion of second arched frame 200. Receiving mechanism 130 may be
a bar that spans the lingual portion of second arched frame 200. In
particular embodiments, hook 405 may engage receiving mechanism 130
to adjust the forward position of arched frame 100 relative to
second arched frame 200. In certain embodiments, this adjustment
may help to prevent a user from snoring when the dental device is
inserted in the user's mouth.
[0137] FIG. 28 illustrates an example dental device comprising a
universal coupler and an example dental attachment. As shown in
FIG. 28, a dental device is provided comprising an arched frame
100, a moldable tray 135, a second arched frame 200, and a second
moldable tray 235. Arched frame 100 may comprise a universal
coupler comprising a substantially planar surface 145. In
particular embodiments, a substantially rounded projection 415 may
be configured to engage the universal coupler. In particular
embodiments, rounded projection 415 may be the only point of
contact between the user's upper and lower dental arches to prevent
a user from clenching his jaw when the dental device is inserted in
the user's mouth. In particular embodiments, rounded projection 415
may contact an opposing arch or may contact one or more incisors of
the opposing dental arch to prevent a user from clenching his jaw
when the dental device is inserted in the user's mouth. The
opposing arch may have a contact surface that may be planar.
[0138] The universal oral appliance comprising a universal coupler
may provide several advantages for a user. In particular
embodiments, a universal oral appliance comprising a universal
coupler may offer more use options to a user. For example, a user's
appliance may be fitted with several different dental attachment
options. The user may choose which dental attachment is best suited
for his situation without having to hire a lab to construct another
appliance. In particular embodiments, a particular user may also
adjust the dental attachment to better suit the shape and size of
the user's mouth. This disclosure contemplates the universal oral
appliance being created from parts in a kit. A user may purchase
the kit instead of a dental device created in a laboratory.
[0139] FIG. 29 illustrates an example arch comprising a dental
attachment. As shown in FIG. 29, an arch is provided that comprises
an arched frame 100 and a moldable tray 135 coupled to arched frame
100. Arched frame 100 comprises an arched body 105 that defines a
plurality of apertures 110. The arch may further comprise a dental
attachment configured to engage arched frame 100. In particular
embodiments, the dental attachment is configured to engage arched
frame 100 along the midline of arched frame 100. In particular
embodiments, the dental attachment may comprise a post 500 and an
anchoring element 505. Post 500 may be coupled at a first end to
anchoring element 505. In particular embodiments, a second end of
post 500 may engage arched frame 100. In some embodiments, post 500
may be configured to removably engage arched frame 100. In
particular embodiments, anchoring element 505 may include a buckle,
a slot, a clasp, a clamp, and/or any other appropriate element to
anchor a tension element. In some embodiments, anchoring element
505 may be configured to be outside a user's mouth when the arch is
inserted in the user's mouth. In some embodiments, the dental
attachment may further comprise a release mechanism 510. As an
example and not by way of limitation, release mechanism 510 may be
a button or a latch. Although this disclosure describes certain
types of release mechanisms 510, this disclosure contemplates any
suitable release mechanism 510. Although this disclosure describes
an arch comprising arched frame 100, moldable tray 135, and a
dental attachment, this disclosure contemplates a one-piece arch
comprising a dental attachment.
[0140] FIG. 30 illustrates an example arch comprising a second
anchoring element and a tension element. As shown in FIG. 30, an
arch is provided that comprises an arched frame 200 and a moldable
tray 235 coupled to arched frame 200. Arched frame 200 comprises an
arched body 205 that defines a plurality of apertures 210. The arch
may further comprise a second anchoring element 245. In particular
embodiments, second anchoring element 245 may be coupled to the
arch along the midline of the arch. The arch may further comprise a
tension element 515. In particular embodiments, tension element 515
may be flexible and may be configured to engage second anchoring
element 245. In particular embodiments, tension element 515 may be
further configured to couple to an anchoring element outside a
user's mouth when the arch is inserted in the user's mouth. In some
embodiments, tension element 515 may comprise a strap 520 and a
coupler 516. Coupler 516 may be configured to engage the second
anchoring element. In particular embodiments, coupler 516 may be
configured to removably engage the second anchoring element. Strap
520 may be coupled to coupler 516. In particular embodiments, strap
520 may be configured to engage the anchoring element outside the
user's mouth when the arch is inserted in the user's mouth. In
particular embodiments, strap 520 may comprise a hard plastic,
leather, or metal. In certain embodiments, strap 520 may be a zip
tie. In other embodiments, strap 520 may be a wire, belt, string,
or any other appropriate element to engage the anchoring element.
Although this disclosure describes an arch comprising arched frame
200, moldable tray 235, and tension element 515, this disclosure
contemplates a one-piece arch comprising tension element 515.
[0141] FIG. 31 illustrates an example dental device comprising a
dental attachment, a second anchoring element, and a tension
element. As shown in FIG. 31, a dental device is provided that
comprises an arched frame 100 and a second arched frame 200. The
dental device further comprises a moldable tray 135 coupled to
arched frame 100 and a second moldable tray 235 coupled to second
arched frame 200. The dental device may further comprise a dental
attachment configured to engage arched frame 100. In particular
embodiments, the dental attachment may comprise a post 500 and an
anchoring element 505. The dental device may further comprise a
second anchoring element 245. Second anchoring element 245 may be
coupled to second arched frame 200. The dental device may further
comprise a tension element 515. Tension element 515 may be
configured to engage second anchoring element 245. In particular
embodiments, tension element 515 may comprise a coupler 516 and a
strap 520. In particular embodiments, strap 520 may be configured
to engage anchoring element 505 outside the user's mouth when the
dental device is inserted in the user's mouth. Anchoring element
505 may be configured to secure substantially the length of strap
520 engaged to anchoring element 505. In particular embodiments,
increasing the length of strap 520 engaged to anchoring element 505
will adjust the forward position of arched frame 100 relative to
second arched frame 200. In particular embodiments, the dental
attachment may further comprise a release mechanism 510.
[0142] FIG. 32 illustrates an example dental attachment and tension
element. As shown in FIG. 32, a dental attachment is provided
comprising a post 500 and an anchoring element 505. Anchoring
element 505 may be coupled to an end of post 500. A tension element
is also provided comprising a strap 520. Strap 520 may be
configured to engage anchoring element 505. Anchoring element 505
may be configured to secure the length of strap 520 engaged to
anchoring element 505. In particular embodiments, the dental
attachment may comprise a release mechanism 510. Release mechanism
510 may be configured to release strap 520 from anchoring element
505.
[0143] FIG. 33 illustrates an example dental device in a user's
mouth. As shown in FIG. 33, a dental device is provided that
comprises an arched frame 100, a second arched frame 200, a
moldable tray 135 coupled to arched frame 100, and a second
moldable tray 235 coupled to second arched frame 200. Moldable tray
135 may comprise a channel 140 configured to engage at least some
of the teeth of the user's maxillary arch 305. Second arched frame
may comprise a second arched body 205 that defines a second
plurality of apertures 210. The dental device may further comprise
a dental attachment. The dental attachment may comprise a post 500
and an anchoring element 505. Anchoring element 505 may be coupled
to an end of post 500, and a second end of post 500 may be
configured to engage arched frame 100. Anchoring element 505 may be
configured to be outside the user's mouth when the dental device is
inserted in the user's mouth. The dental device may further
comprise a second anchoring element 245 coupled to second arched
frame 200. The dental device may further comprise a tension element
comprising a coupler 516 and a strap 520. Coupler 516 may be
configured to engage second anchoring element 245. Strap 520 may be
coupled to coupler 516 and may be configured to engage anchoring
element 520 outside the user's mouth when the dental device is
inserted in the user's mouth. Anchoring element 505 may be
configured to secure substantially the length of strap 520 engaged
to anchoring element 505. In particular embodiments, increasing the
length of strap 520 engaged to anchoring element 505 may adjust the
forward position of arched frame 100 relative to second arched
frame 200. In particular embodiments, adjusting the forward
position of arched frame 100 relative to second arched frame 200
may adjust the forward position of the user's maxillary arch 305
relative to the user's mandibular arch 300. In particular
embodiments, adjusting the forward position of the user's maxillary
arch 305 relative to the position of the user's mandibular arch 300
may help to improve the user's breathing and/or prevent the user
from snoring.
[0144] In particular embodiments, the dental device comprising a
dental attachment and a tension element may allow a third party
faster access to a user's mouth and airway. For example, if the
user is a patient sleeping in a sleep laboratory, a doctor in the
laboratory may quickly pull on the tension element to open an
airway that closed while the patient slept. As another example, if
the user is a patient undergoing surgery in a hospital, a surgeon
may quickly release the tension element to open the patient's mouth
for intubation or for insertion of an instrument while the patient
is sedated. In particular embodiments, the dental device comprising
a dental attachment and a tension element may pull the user's lower
jaw forward without locking the lower jaw in place. The user's
lower jaw will maintain a certain range of lateral motion while the
dental device is inserted in the user's mouth. This disclosure
contemplates the dental device comprising a dental attachment and a
tension element being created from a kit. A patient, doctor, or
surgeon may purchase the kit and create the dental device quickly.
In particular embodiments, the dental device may be a disposable
device that may be thrown out after one or more uses.
[0145] FIG. 34 illustrates an example process for creating a dental
device. At step 600, an arched frame is formed. In particular
embodiments, the arched frame may be configured to be positioned
proximate to the occlusal surface of a user's dental arch such that
the arched frame extends beyond the cuspids of the user's dental
arch. The arched frame may define a plurality of apertures. At step
605, an adjustment mechanism is coupled to the arched frame. In
particular embodiments, the adjustment mechanism may comprise a
hook and a threaded adjustor. At step 610, a moldable tray is
formed. In particular embodiments, the moldable tray may comprise a
channel configured to engage at least some of the teeth of the
user's dental arch. In some embodiments, the channel may be shaped
to conform to the teeth of a generic user's dental arch. In other
embodiments, the channel may be a smooth channel configured to
cover some of the teeth of the user's dental arch. In particular
embodiments, the channel may be further shaped to conform to a
particular user's dental arch. At step 615, the moldable tray is
coupled to the arched frame. In particular embodiments, the
moldable tray may engage the plurality of apertures. In particular
embodiments the process may be repeated to form a second arched
frame and a second moldable tray. In particular embodiments, the
arched frame may comprise kevlar polycarbon, acryllic,
polycarbonate resin thermoplastic, or any other suitable hard
plastic polymer. In particular embodiments, the moldable tray may
comprise polycaprolactone.
[0146] In particular embodiments, the process illustrated in FIG.
34 may lead to faster creation and production of dental devices.
Users may avoid sending dental impressions to a laboratory to
create a dental devices thus saving time and money.
[0147] Although example steps are illustrated and described, the
present invention contemplates two or more steps taking place
substantially simultaneously or in a different order. For example,
step 605, coupling an adjustment mechanism to the arched frame, may
be performed after step 610, forming a moldable tray. In addition,
the present invention contemplates using methods with additional
steps, fewer steps, or different steps, so long as the steps remain
appropriate for creating a dental device.
[0148] Various embodiments disclosed herein may be used together in
a variety of combinations. For example, in certain embodiments, the
various posts, such as posts 802 and 882, may be coupled to any of
the various oral appliances disclosed herein, including the oral
appliances disclosed in U.S. Pat. No. 7,748,386. As another
example, the various posts described herein may be coupled to any
of the various masks disclosed, such as but not limited to masks
850, 890, 892, and 894. As another example, in certain embodiments,
the various adjustment mechanisms may be used with the various oral
appliances disclosed herein, including the adjustment mechanisms
and oral appliances disclosed in U.S. Pat. No. 7,748,386. As
another example, in certain embodiments the various oral appliances
may be coupled with the various dental attachments disclosed
herein.
[0149] Although the present invention has been described above in
connection with several embodiments, changes, substitutions,
variations, alterations, transformations, and modifications may be
suggested to one skilled in the art, and it is intended that the
present invention encompass such changes, substitutions,
variations, alterations, transformations, and modifications as fall
within the spirit and scope of the appended claims.
* * * * *