Abstract: A dynamic infant head support for preventing, or correcting, the abnormal shape of a head of an infant, and a method of using the support for treating deformational plagiocephaly. The support is an oval-shaped pillow, with a central opening to receive the head of the infant to be treated. Spaced barriers divide the interior of the pillow into a plurality of compartments. A ring-like manifold passes through the pillow and communicates with each compartment. A plurality of valves is operatively associated with the manifold; one valve is located in each compartment. The valves allow fluid, such as pressurized air, in the manifold, to inflate individual compartments. The manifold is pressurized by a pump, at a remote location. A remote controller is connected to the valves by electrical leads for governing the sequence of operation of the valves, and regulating the duration of time that each valve is open.

Abstract: The invention relates to an inserter for an intrauterine system, comprising a handle (3) having a longitudinal opening (8) at its first end, said opening (8) having a longitudinal axis parallel to the longitudinal axis of the inserter, a first end (8a) and a second end (8b), a movable slider (5) arranged in said longitudinal opening (8) and having a first end (5a) and a second end (5b), a plunger (2) attached to the handle (3), an insertion tube (6) arranged around the plunger (2) having a first end and a second end, with its second end attached to the slider (5), wherein the inserter further comprises locking means for reversibly locking the intrauterine system in relation to the plunger (2) via a removal string of the intrauterine system, said locking means being controllable by the slider (5) and/or the insertion tube (6).

Abstract: A surgical shield includes an at least partially rigid shield member extending in at least two spatial dimensions, at least one flexible sheet member, and a coupling element. The shield member has an aperture traversable by a surgical instrument, while the coupling element is provided on the shield member for releasably connecting the shield member to the instrument. The flexible sheet member is attached to the shield member so as to define, with the shield member, an enclosure having one open side opposing the shield member.

Abstract: A tongue grasping and restraining device holds the tongue securely during sleep in order to minimize the risk of the tongue slipping back and blocking the throat, a condition known as obstructive sleep apnea. Plural tongue gripping projections are coupled to upper and lower supports. The projections engage and hold the tongue. The upper and lower supports are biased toward one another into a tongue engaging position. The upper support is coupled to the user's upper jaw, for example, to a denture, dental appliance or by upper teeth engaging mechanisms. The lower support can be hinged or otherwise joined to the upper support or can be separate therefrom. A tube and rod mechanism in one embodiment couples the upper and lower supports together. Exemplary methods of manufacturing tongue gripping projections are also disclosed.

Abstract: A dental guard system for fitting boil and bite dental guards so that undesirable deformations of the guard are avoided during the fitting of the guard to the user. The system includes a boil and bite dental guard and an associated forming tray configured to be generally rigid but conformable in that it tends to retain its shape so as to inhibit undesirable deformations of the guard, yet enables the guard to form to the teeth of the user.

Abstract: An orthopedic knee brace includes an upper medial upright; a lower medial upright; an upper lateral upright; a lower lateral upright; a medial hinge connected rotatably to the upper and lower medial uprights; a lateral hinge connected rotatably to the upper and lower lateral uprights; and wherein one of the medial and lateral hinges is configured such that its respective uprights rotate from a flexion to an extended relative positioning while striking a radially-decreasing arc, while the other of the medial and lateral hinges is configured such that its respective uprights rotate from a flexion to an extended relative positioning while striking a radially-increasing arc.

Abstract: A nasal cannula includes a cannula body having a passageway extending therethrough from a first end to a second end and an airflow restrictor coupled to the cannula body and positioned to selectively restrict air flow through the passageway during exhalation. A flow regulator is settable to a plurality of airflow positions and cooperates with the airflow restrictor to regulate the air flow during exhalation such that the air flow during exhalation is variable in response to the airflow position of the flow regulator. In one embodiment, an airflow restrictor is deformable from an at-rest configuration to an inhalation configuration during inhalation, and exerts a substantially constant backpressure during exhalation for a predetermined range of expiration flow rate. Methods of use are also provided.

Abstract: A respiratory mask assembly includes a respiratory mask including a mask shell and a mask cushion, a forehead support adjustably coupled to the mask, and an angular adjustment member. The forehead support includes a joining member provided to the mask shell and a cushion frame pivotally mounted to the joining member. The cushion frame is adapted to be selectively locked against pivotal movement in at least three predetermined angular positions relative to the joining member by a tongue and slot arrangement. The angular adjustment member allows relative angular adjustment between the cushion frame and the joining member. The angular adjustment member includes a pair of flexible arms that are adapted to be flexed towards one another to disengage the tongue from a respective one of the slots, and releasing the flexible arms allows the flexible arms to resiliently flex away from one another to engage the tongue and the respective slot.

Abstract: An orthotic device for correcting an abnormality in a newborn baby's neck includes a three element rigid or semi-rigid support member. The support member includes three elements, each in the shape of a frustum of a cone with one element stacked on top of another. The first or bottom element has a larger open base and a smaller upper portion and flares outwardly from top to bottom from vertical by about 20°. The middle element flares outwardly from bottom to top by about 20° and is superimposed on the first element. However, the second element is rotatably fixed to the first element and is rotatable in about one mm increments. The upper element flares outwardly from vertical by about 45°. A method for correcting an abnormality in a newborn's neck in one mm increments per day using the aforementioned device is also disclosed.

Abstract: Contraceptive and/or sterilization methods and devices are disclosed which may improve the speed of tubal occlusion and mechanisms for anchoring for a contraceptive device. In accordance with some embodiments, improvements may be made to the delivery catheter to induce trauma and create faster tubal occlusion, improvements may be made to the occlusion device to prevent migration and induce trauma, and improvements may be made to the occlusion device to reduce the total volume of in-growth required compared to conventional expansive occlusion devices.

Abstract: A mouth guard composed of a polymer consisting essentially of polycaprolactone exhibits a low softening point, enabling it to be easily custom-fitted by the user or a health professional. The material is provided in the form of a generally U-shaped, unformed sheet of material, enabling the material to be heated with hot water or microwave energy and custom-fitted to the dentition of a user. The mouth guard may be perforated and may include a no-stick layer and/or a flavoring agent. A plurality of mouth guards may be provided in different sizes for children and adults and different shapes for different sports. In the preferred embodiments the mouth guard has a periphery including a plurality of lobes and cusps to enhance fitting. A method of fabricating an improved mouth guard according to the invention is also disclosed.

Abstract: Provided is an incurvated-nails and ingrown-nails correcting device that uses a magnetic force and that is capable of adjusting the space between a magnet and a magnetic sheet that is placed on a nail. The subject device includes a magnetic sheet that is placed on a nail; the device's main part that includes a body that is attached to the magnetic sheet by using an adhesive agent or by using the magnetic force of the magnet, an arm that extends outward from the body, a head that is arranged at the edge of the arm, and a joint by which the arm is rotatably connected to the body and by which the head is rotatably connected to the arm; and a magnet mounted on the head.

Abstract: An implant for treating an obstructive airway disorder includes an elongate implant body configured for implanting in airway-interface tissue. At least a portion of the elongate body carries a light transmission material for permitting light transmission therein. Systems and methods of treating an airway disorder including implanting an implant in an airway-interface tissue are also provided.

Abstract: The present invention relates to the field of assisting sleep, including apparatus and methods for assisting sleep. In one form, the invention provides a postural support apparatus comprising a first supporting means (5) adapted to support the head of the user, a second supporting means (15) adapted to support the rib cage of the user, and a recess (3) intermediate the first supporting means (5) and the second supporting means (15), the recess (3) being adapted to accommodate at least part of an arm of the user, wherein the apparatus aligns the head and spine of the user such that the user's airways are kept open.

Abstract: An intra-oral device for positioning oral tissues during medical treatment, for example, radiation treatment. The device includes upper and lower dental arch members configured to engage the maxillary and mandibular teeth or edentulous arch(es) of a patient, respectively. The upper and lower dental arch members are operatively coupled to provide a dental arch assembly. A protective element to displace or depress a patient's tongue is secured at a suitable working position with respect to the dental arch assembly. In an embodiment, provision is made for three-dimensional spatial adjustment of the protective element to a desired location, at least during initial fitting and assembly. The device is then secured to allow consistent repetition of the oral tissue positioning from treatment to treatment. The protective element may be configured to engage the tongue of a patient so that the tongue may be selectively positioned for treatment and/or diagnostic procedures.

Abstract: A device includes a rolled tubular section and at least two strips rolled together with the tubular section. The strips extend from a rim of the tubular section and are spaced a distance apart from each other, with at least a portion of an inside area of the tubular section provided with an adhesive. When rolled, the adhesive on the inside area of the tubular section contacts at least a part of one of the two strips and the two strips form a path along the tubular section. Each of the two strips has a release layer that is configured to provide each of the two strips with a release value away from the adhesive on the inside of the tubular section of between 15-50 dynes.

Abstract: In some embodiments, an implant delivery device can include a housing defining a housing passageway. A distal end of the housing can flexibly couple to a head that can define a head passageway. Collectively, the housing passageway and the head passageway can define an insertion passageway such that, at least a portion of the insertion passageway is nonlinear. The implant delivery device can include at least one insertion member having a distal end configured to be removably coupled to an implant. The insertion member can be disposed within the housing such that, at least a portion of a proximal end of the insertion member is housed within the housing. The insertion member can be configured to bend, pivot, and/or rotate and move within a portion of the insertion passageway to convey the implant to a target tissue.

Abstract: A support shell arrangement (20) is provided for arranging on a lower leg, having a foot part (23) and a calf part (21). The calf part includes two calf struts (29, 30) disposed at the side of an entry opening (32) of the calf part, extending in the longitudinal axis of the calf part, and a heel strut connected to the calf struts in a strut connection and extending toward a heel part of the foot part. A support bow arrangement (24) has two bow struts (34, 35) extending in a U-shape about a sole area, the free strut ends thereof being pivotally connected in pairs in a common pivot joint (43, 44) on a joint axis corresponding to the ankle joint and connected to a calf strut, and connected to each other in a V-shape by a common support basis (36). The support base is pivotally connected to the heel strut of the calf part at the heel side end thereof.

Abstract: A medical device configured for assistance with the cervical cerclage procedure is provided. The medical device includes a barrier structure with a finger and a therebetween. A hub is fixed to a distal end of the catheter and defines an extension with a second void between an end surface of the hub and the extension. The barrier structure and the hub are releaseably attached with the extension disposed within the first void and the finger within the second void. A wire guide withdrawably extends through coaxial holes within the hub, extension, finger, and a portion of the barrier structure to fix the hub and barrier structure together.

Abstract: Systems and apparatuses for administering reduced pressure treatment to a tissue site include a reduced pressure source, a drape having a plurality of projections for contacting the tissue site, and an adhesive connected to at least a portion of the drape for sealing the drape to a portion of a patient's intact epidermis.