Abstract: An orthopedic device comprises a main body defining an outer surface and a cuff extending from an end portion of the main body with frictional material disposed on an inner surface of the first cuff. A hinge is connected to the main body and terminates along the main body short of the cuff. The cuff is arranged to fold over the outer surface of the main body in a disengaged configuration, such that the outer surface of the first cuff is adjacently against the outer surface of the main body.

Abstract: A wound dressing material comprising a solid substrate having interstitial spaces therein, wherein said substrate is a hydrophilic open-cell foam material, and wherein said interstitial spaces are at least partially filled by a hydrophilic polyurethane foam different from said substrate foam material. Also provided is a method of making a porous wound dressing material comprising the steps of: providing a substrate of a solid hydrophilic first foam material; applying a fluid or gel polyurethane foam prepolymer mixture to at least one surface of said solid substrate; and curing said prepolymer in contact with said solid substrate.

Abstract: Bandage apparatus, methods, and antimicrobial bandages for facilitating wound healing by providing an antimicrobial functionality. A bandage apparatus includes a substrate with a first surface and a second surface opposing the first surface. An attachment mechanism and a nanostructure film are provided on the first surface. The attachment mechanism facilitates removably attaching the substrate to a part of a body comprising a wound. The nanostructure film includes a plurality of nanostructures that contact the wound without puncturing the wound when the substrate is attached to the part of the body comprising the wound.

Abstract: A device for treating carpal tunnel syndrome of a person's hand, which has a palmar aspect, with thenar and hypothenar regions, and a dorsal aspect opposite the palmar aspect. The cuff has a C-shaped profile in cross section, wherein two ends of the C-shaped profile of the cuff form the cuff opening. The cuff is formed from two or more cuff parts, wherein these cuff parts have a C-shaped profile in cross section and are connected to each other by means of a connection element to form the cuff. The cuff parts are preferably connected to each other, by means of the connection element, in a movable and/or pivotable and also releasable manner, such that the width of the cuff opening can be individually adapted for each patient. This results in simple, efficient and safe treatment and handling of the cuff according to the invention or of the device.

Abstract: A conformable body interface is fabricated using a data set representing a three-dimensional, soft tissue body surface. The conformable body interface includes a body scaffold that is divided into two or more longitudinal segments separated by axial joints. Optionally, the body scaffold is further divided into two or more circumferentially split segments separated by circumferential joints. The axial joints are circumferentially constrained by elastic bands, tabs, or similar structures and the circumferential joints are longitudinally constrained by elastic axial tethers or similar structures. In this way, the body interfaces can accommodate swelling and bending of the body surface.

Abstract: The invention relates to a brace for use with animals. The brace comprises an upper structure, a lower structure, a first reinforcement positioned to a first lateral side of a longitudinal axis of the upper structure, and a second reinforcement positioned to a second lateral side of the longitudinal axis of the upper structure. Each of the first reinforcement and second reinforcement are integral to the upper structure and parallel to the longitudinal axis. The lower structure is independent of and releasably secured to the upper structure.

Abstract: A surgical drape for a patient side cart of a teleoperated surgical system may include a body and an attachment device feature. The body may be sized and shaped to cover at least a portion of an arm or main column of the patient side cart. The attachment device feature may be connected to the body. The attachment device feature may be configured to install the surgical drape to the arm or main column so as to cover at least a portion of the arm or main column with the surgical drape. The attachment device feature may be detectable by a sensor in an installed position of the surgical drape on the arm or main column. At least one of the main column and the arm may include a sensor to detect an attachment device feature of a surgical drape.

Abstract: A surgical robotic drape for enveloping a surgical robotic arm includes a covering for enveloping the robotic arm to define a sterile boundary thereover; an interface element attached to the covering, the interface element being configured to engage a drive assembly interface and an instrument interface to couple the drive assembly to an instrument to thereby provide drive to the instrument through the drape; and a guiding structure attached to the covering for locating the interface element relative to the drive assembly interface. The guiding structure is deformable between a storage configuration for when the drape is to be stored, and an operative configuration in which the guiding structure is configured to attach to the robotic arm to position the interface element with respect to the interface of the drive assembly for engagement therewith.

Abstract: A neck collar can include a unitary foam pillow having extending from a first side first and second collar straps that extend opposite one another and terminate in respective distal ends separated by a space having a first distance in a relaxed state. The neck collar can also include an elastically deformable spring member embedded in the unitary foam pillow, the elastically deformable spring member being generally C-shaped in the relaxed state and having portions extending into both of the first and second collar straps. The elastically deformable spring member can be deformed such that the first distance is increased to a second distance.

Abstract: An inserter is provided which includes a handle having an upper cover and a bottom cover, the upper cover having a longitudinal opening, a proximal end and a distal end; a mounting member extending from an inner surface of the bottom cover of the handle, the mounting member having a through-hole; an inner tube having a proximal end and a distal end, the proximal end of the inner tube attached to the mounting member; an insertion tube movably coupled to the inner tube with a longitudinal axis essentially parallel to a longitudinal axis of the inner tube; a switch coupled to a proximal end of the insertion tube and arranged in the opening; and a string having a proximal end removably coupled near the proximal end of the opening, a distal end of the string coupled to a device to be inserted inside a human anatomy.

Abstract: A shoulder immobilizer (20) includes a semi-rigid or rigid orthosis, in the form of an arm support (22), which supports the upper arm, elbow, forearm and wrist of a patient. A bolster (24) is positioned between the patient and the arm support (22). A body strap (26) extends around the patient and attaches to the arm support (22) and/or the bolster (24), holding the arm support and bolster in position against the body of the patient. In embodiments, the shoulder immobilizer (20) may utilize a shoulder strap (28), but such a shoulder strap is not necessary for shoulder immobilization of the patient.

Abstract: A stockinette (200), suitable for covering an appendage (1440) of a patient, includes one or more folds (206). The fold (206) can be in a length of material (205) disposed between an open end (204) and a closed end (203). Alternatively, the fold (880) can be in an optional cuff (860) formed by a section of material (661) near the open end (603). Folds can be present both in the length of material (205) and in the cuff (860) as well. The cuff (860) can be disposed atop the fold (206) in the length of material (205). The stockinette (200) enables one person to apply the stockinette (200) to an appendage (1440) with one continuous motion that expands the folds.

Abstract: Oral treatment devices formed from wax-based compositions that are thermally stable when formed into a three-dimensional shape to a temperature of at least 45° C. and plastically deformable at room temperature (25° C.). The wax-based compositions include a wax fraction homogeneously blended with a polymer fraction. The wax fraction includes at least one wax. The polymer fraction includes at least one polymer selected such that, when the wax and polymer are homogeneously blended together, they yield a wax-based composition having the desired properties of thermal stability and plastic deformability. Oral treatment devices are dimensionally stable to a temperature of at least 40° C. without external support and can be plastically deformed in a user's mouth to become at least partially customized to the size and shape of user's unique dentition and/or an appliance in a user's mouth.

Abstract: The present embodiments provide a brace which includes an actuator. The actuator provides movement of the arm and shoulder, abduction movement, so that during recovery from shoulder surgery, the shoulder and arm movement may be supported in increased range of motion positions. This may be done with a single brace rather than requiring multiple braces during the recovery process.

Abstract: A breakaway device for a mouthguard is provided, having a lanyard assembly couplable to a mouthguard assembly. The lanyard assembly includes a mouthguard tether couplable to the mouthguard assembly, and a neck tether that can be worn around a user's neck. The lanyard assembly also includes front and rear breakaway connectors, such that when a tensile force is exerted on the mouthguard tether or the neck tether, one or both of the breakaway connectors detaches before the mouthguard tether or neck tether separates.

Abstract: Provided is a multi-layered non-woven wound dressing produced by a method including steps of: preparing multiple natural polymeric layers; stacking the multiple natural polymeric layers to form a polymeric structure; preparing multiple natural polymeric threads; and stitching the polymeric structure with the natural polymeric threads to enforce a formed multi-layered non-woven wound dressing and continuous crossing lines to enforce the formed multi-layered non-woven wound dressing to reinforce its longitudinal and transversal tensile strength for a pre-set period of degradation in wound.

Abstract: A method of treating sleep disorder breathing in a patient, the method comprising in a first step providing a set of oral appliances comprising a first and at least a second oral appliance (30). Each of the first and at least second oral appliances comprises a generally U shaped appliance body including an inner wall (34), an outer wall (36), and a web (38) interconnecting the inner wall and the outer wall. The web has a front section and two arms with trailing ends. The web comprises at least one breathing hole (80) so as to define a total cross sectional area for breathing and the total cross sectional area for breathing of the first oral appliance is larger than the total cross sectional area for breathing of the second oral appliance. In a second step, a patient wears the first oral appliance in a first treatment stage whilst sleeping for a first period of time and in a third step the patient wears the second oral appliance in a second treatment stage whilst sleeping for a second period of time.

Abstract: A rear sheet adjustment assembly of neck collar is provided, including a nape base and a support sheet. The nape base includes a main body, at least one stopper, a positioning member and a plurality of openings. The at least one stopper is connected with the main body and defines an inserting space therebetween. The positioning member is disposed on the main body. The positioning member has a first combination portion. The support sheet is adapted for supporting a nape of a neck and movably inserted within the inserting space. The support sheet has a plurality of second combination portions, and each of the second combination portions is adjustably engageable with the first combination portion.

Abstract: Wound treatment materials can have at least two perforated biomatrix layers which are interconnected. Methods for preparing such wound treatment materials include the application of adhesives. Treatment of exuding wounds, and vacuum-assisted wound treatment therapy, can be carried out with the wound treatment materials.

Abstract: An oral device for preventing sleep apnea is provided. The oral device maintains an opening between the anterior teeth, resulting in a wider upper airway, while allowing the mouth to also open for yawning and normal talking. The oral device provides an upper plate and lower plate, each adapted to retain the biting surface of the respective set of maxilla and mandible teeth, wherein curved rods pivotally interconnecting both plates are adapted for maintaining an operable spaced apart relationship therebetween. The oral device is a unitary construction made from FDA-approved elastomers.