Abstract: Provided is a mandibular advancement system including: an upper teeth seating part on which upper teeth of a user is placed; a lower teeth seating part on which lower teeth of the user is placed; a driver connected to the upper teeth seating part and the lower teeth seating part and configured to change a relative location of the lower teeth seating part with respect to the upper teeth seating part; a detector configured to detect biometric information of the user; and a controller configured to control driving of the driver based on the biometric information provided by the detector, wherein the driver is disposed outside an oral cavity of the user.

Abstract: A hemostatic surface application device having a region of hemostatic foam for contact with a patient's skin where a wound exists or is created, the device includes: a release layer, the release layer in contact with a hemostatic flexible foam section, and a structural foam layer having a front side and a back side surrounding the hemostatic flexible foam layer, forming a generally central hemostatic surface exposed through the front side of the surrounding structural foam layer, and a support layer adhered to the backside of the structural foam layer.

Abstract: A releasable medical drape, and systems and methods having the same, includes at least a liquid-impermeable, vapor-permeable layer, a pressure-sensitive adhesive layer, and a soft-gel layer having a plurality of apertures. The soft-gel layer is configured to be disposed adjacent to a tissue site. A portion of the pressure-sensitive adhesive layer extends through the plurality of apertures in the soft-gel layer to contact the tissue site. The soft-gel layer forms a good seal with the tissue site and the pressure-sensitive adhesive layer extending through the plurality of apertures forms a firm—but releasable—coupling with the tissue site.

Abstract: A suboccipital compression pad may include a pad member configured to contact a suboccipital region of a patient. A suboccipital compression pad may include a pair of securing straps extending respectively from opposing ends of the pad member, the pair of securing straps having proximal ends diverging into upper rear straps and lower rear straps to form an open space between the upper rear straps and the lower rear straps such that portions of the upper rear straps are located above ears of the patient and portions of the lower rear straps are located below ears of the patient without covering ears of the patient, wherein one of the upper rear straps and the lower rear straps of the pair of securing straps is configured to be selectively attachable to different locations of a back side of the pad member.

Abstract: A microstructured hemostat comprising multiple layers of microstructure, each layer characterized by one or more length scales, is described. Microstructured hemostats of the present invention, can reduce the time for blood coagulation, control the morphology of the coagulation, and provide a novel diagnostic platform for evaluation of coagulation function from a morphological perspective.

Abstract: A composite moldable splint and method for using the same is described. In some embodiments, the splint has at least a partially fluid-filled inner volume, which in some embodiments may include foam, rubber, water, or pelletized material, enclosed by a flexible liner, surrounded by a thermoplastic layer that is flexible and moldable when heated. The inner volume, which may include a thermoactive adhesive having differing viscosity characteristics at a plurality of temperatures, provides the ability to mold the cushion into a wide range of shapes and contours, such as when forming around a body part. The thermoplastic layer provides the ability of the cushion to be molded when heated, while the inner volume tends to maintain a shape, and allows the thermoplastic layer to stay in its formed shape as the cushion cools. The cushion may be used in a range of medical applications for stabilizing patients and body parts.

Abstract: Systems, kits, methods of manufacturing, and a sealing member for creating a sealed space are described. The sealing member can include a film layer and a first adhesive layer coupled to the film layer. The sealing member can also include a second adhesive layer coupled to the first adhesive layer. A plurality of apertures may extend through the second adhesive layer. Each aperture can expose at least a portion of the first adhesive layer through the second adhesive layer. A plurality of polymer particles may be disposed in the first adhesive layer. The polymer particles can be configured to dissolve in response to interaction with a switching solution.

Abstract: A wound debridement system includes a wound dressing having an active layer and a wound interface layer. The active layer is formed from one or more transmission layers that are arranged about a central post. Activation of the transmission layers is configured to cause the movement of the wound interface layer relative to a tissue site to which the wound dressing is applied. A drive unit is operably attached to the central post. The drive unit is configured to generate and transfer a vibrational energy and/or a rotational movement to the transmission layer(s) via the central post. The resultant vibration and/or rotation of the transmission layer(s) is imparted onto the wound interface layer, thereby effectuating the desired movement of the wound interface layer relative to the tissue site, which allows for the debridement of debris that may be located at the tissue site.

Abstract: A bandage has a plurality of prongs extending from a portion of a bottom side of the bandage base. A depression region can be formed on the top side of the bandage base, opposite the plurality of prongs, where depressing the depression region can cause the prongs to interact with the user's skin, typically at a wound site. The depression region can be a raised dome having a button in a center region thereof, wherein depressing the raised dome beyond a given depth causes the raised dome to press the plurality of prongs against the skin of the user and automatically move back to its undepressed configuration. The prongs can have sufficient sharpness to create a slightly unpleasant sensation but can be dull enough not to create any damage to skin. Such counter irritation can provide an analgesic effect for the user.

Abstract: Semi-rigid bandages disclosed herein include a bandage structure layer with an embedded resin material. The resin material is formulated to cure when exposed to an activator such as air or water. Upon curing, the bandage hardens to a semi-rigid state that is harder and more rigid than conventional bandage materials found in household first-aid kits, yet less rigid than fiberglass-based orthopedic casts.

Abstract: The present wrist brace includes an advantageous lacing configuration that provides a cast-like compression on a patient's forearm, wrist, and hand. Pulling the lacing mechanism equilibrates lace tension along the length of the wrist brace in a way that applies consistent compression to the patient's forearm and wrist.

Abstract: A two layer compression garment measuring system that displays a pressure indicia when the garment is stretched, wherein the pressure indicia is displayed by moving from a position under an opaque layer of material (at low or no pressure) to a position under a window or transparent or translucent layer of material (at higher pressure). When the indicia can be seen by an observer through the window or transparent or translucent layer, then the higher pressure has been reached. The viewed indicia optionally displays the pressure level. In various optional designs, the location of attachment between the two spaced-apart locations is adjustable, or the length of the upper layer is adjustable such that the attachment location can be aligned with the indicia. A design having a free ended upper layer is also included.

Abstract: A dressing configured to be positioned adjacent to a tissue site is disclosed herein. The dressing may include oxidized regenerated cellulose (ORC), collagen, and at least one nutrient including glutamine. Methods of treating a tissue site are also disclosed herein.

Abstract: A reduced-pressure treatment system for applying reduced pressure to a tissue site at a limited-access location on a patient includes a reduced-pressure source, a treatment manifold for placing proximate the tissue site and operable to distribute reduced pressure to the tissue site, and a sealing member for placing over the tissue site and operable to form a pneumatic seal over the tissue site. The reduced-pressure treatment system also includes a reduced-pressure bridge and a moisture-removing device on at least portion of the reduced-pressure bridge. The reduced-pressure bridge includes a delivery manifold operable to transfer the reduced pressure to the treatment manifold, an encapsulating envelope at least partially enclosing the delivery manifold and having a patient-facing side, and a reduced-pressure-interface site formed proximate one end of the reduced-pressure bridge.

Abstract: A bandage device having a flexible body with a plurality of fluid reservoirs thereon each containing a liquid topical treatment therein. Mixing areas located between the respective fluid reservoirs on the bandage provide for mixing and formation of liquid mixtures of the respective liquid topical treatments flowing thereto from the respective fluid reservoirs located adjacent thereto. The liquid mixtures from the mixing areas when absorbed through the skin of a wearer of the bandage yield an enhanced synergistic effect exceeding that of the individual fluids such medications or essential oils.

Abstract: Trimmable conformable wound dressings, kits containing the same and methods of using the same. The wound dressings may protect a treatment site from microbial contamination or other disturbances while a wound heals or to enable the application and maintenance of vacuum over the treatment site. The wound dressings may include first and second sections of support layer material on opposite sides of one or more intermediate sections of support layer material. The first and second sections of support layer material meet the intermediate sections of support layer material along peel tab junctions that provide peel tabs.

Abstract: Disclosed herein are embodiments of a wound dressing layer. The wound dressing layer may include an open-cell foam. The foam may have a 50% compression force deflection of not more than about 4.8 kPa. The foam may also have a density of at least 24 kg/m3. The foam may exhibit a density increase of a factor of at least 12 at about ?75 mmHg.

Abstract: Apparatus and methods for a therapeutic boot that promotes the healing of pressures sores is described. Bedridden patients are prone to developing pressure sores over bony prominences of the foot such as a heel. The therapeutic boot includes a sides-down, open door design that provides unobstructed access to a wound site. The therapeutic boot may be designed to offload the patient's heel and bony prominences on both sides of the patient's ankle. The therapeutic boot is designed such that opening and closing the boot does not apply pressure and or friction to the wound site.

Abstract: The splint kit provides a sealed splint, bandaging, and a water source for setting the splint. Different kits may be needed depending upon the size of the user to which the splint will be applied. The kits may also vary according to the body part to be set. The size of each splint is based upon the size of the user and the size of the body part(s) to be splinted to eliminate the need for the user to size the splint. The splint is self-contained in its own packaging to maintain the integrity of the splint. The fiberglass/hardening material is encased by a foam material and/or felt to further simplify the process of applying and setting the splint.

Abstract: Apparatus and methods are described herein for preventing injury to the tongue of a user. An oral device can include a tongue protector configured to be disposed beneath the tongue of a user and having a tongue receptacle configured to receive the tip of the tongue of the user and cover a distal portion of the top surface of the tongue. The oral device can also include a left tooth protector and a right tooth protector configured to be disposed over only the left lower molars and canine and the right lower molars and canine of the user, respectively. A left coupler and a right coupler can couple the left tooth protector and the right tooth protector, respectively, to the tongue protector. The left coupler and the right coupler can be configured to allow limited movement of the tongue protector while retaining the tongue protector in the user's mouth.