A surgical implant, which in use, provides a barrier between layers of tissue such that tissue on one side of the implant does not adhere to tissue on the other side, the improvement comprising that the implant is made of suitably anatomically shaped surgically acceptable sheet material.

A surgical implant, which in use, provides a barrier between layers of tissue such that tissue on one side of the implant does not adhere to tissue on the other side, the improvement comprising that the implant is made of suitably anatomically shaped surgically acceptable sheet material.

In an aspect, the device for stretching skin of a user's neck includes a stretchable body that extends along a first axis, a first end integrally connected to the stretchable body, and a second end integrally connected to the stretchable body. The device further includes an adhesion layer formed on one side of each of the first end and the second end for attaching the device to the skin of the user's neck. Each of the first end and the second end comprises a center part that is integrally formed with the stretchable elongate body, a first extension connected to the center part and extending along a second axis away from the center part, and a second extension connected to the center part opposite the first extension and extending along the second axis away from the center part and the first extension.

A therapeutic device includes a generally rigid but elastically deformable sheet body including a bridge portion, first and second support portions extending outwardly from the bridge portion in opposite directions along a longitudinal dimension, and adhesive or an adhesion member on a first surface along the bridge portion that is adapted for adhesion to skin of a user above a target site. The therapeutic device also includes first and second projections on the first surface proximate to lateral edges of the sheet body. The sheet body is configured to assume a neutral configuration in which the first and second projections space the bridge portion and the adhesive or the adhesion member apart from the target site by an air gap, a depressed position during affixation of the first surface to the target site, and an adhesion configuration after affixation of the first surface to the target site.

The present invention provides an improved bilateral compression device for post-operative surgical site, the bilateral compression device including a central cavity presented by an outerwall and a circumscribing sidewall, the central cavity in receipt of a post-operative pillow further comprising an outer membrane separated from an inner membrane for exerting a central compressive force towards the post-operative surgical area which varies from a surrounding compression force.

The present disclosure relates to a film for oral hemostasis and wound protection and, more particularly, to a film for oral hemostasis and wound protection which, being attached to a wound area in an oral cavity, delays or prevents microbleeds and controls medicinal component release. The film provided by the present disclosure is capable of including a polyol, an alcohol and a biodegradable polymer in the state of partial swelling, thereby locally absorbing blood or pus or arresting hemorrhage. Moreover, due to its high elongation ratio, the film provided by the present disclosure is capable of maintaining its adhesive force even when having blood, saliva and pus absorbed inside an oral cavity and conveniently deforming according to the shape of a seriously corrugated local area, which causes only slight foreign body sensation even after a long period of time of attachment on to the local area. In addition, the film provided by the present disclosure includes a disintegrant which is dissolved and released by reacting with blood to form microchannels that act as paths for drug release and is capable of adjusting the amount and the size of the microchannels, thereby controlling the amount of drug release. The present disclosure doesn't require a patient to detach the film attached inside an oral cavity by hand because the adhesive layer and the backing layer dissolve entirely over time.

A support dressing comprises a conformable material that is capable of conforming to a body part when secured thereto; an adhesive for releasably securing the dressing to the body part; and at least one resilient component that has greater stiffness than the flexible material. It is particularly useful in preventing or reducing undesired torsion, for example, for the neck.

A support dressing comprises a conformable material that is capable of conforming to a body part when secured thereto; an adhesive for releasably securing the dressing to the body part; and at least one resilient component that has greater stiffness than the flexible material. It is particularly useful in preventing or reducing undesired torsion, for example, for the neck.

Apparatus are described for providing support and maintenance of facial structures using facial support members that include internal silicone gel pads that are encased in an elastomeric casing and are dimensioned to apply downward pressure to tissues underlying the facial support members.

A nasal cavity bandage dressing and method of use thereof, including a bandage made from a waterproof, antimicrobial, and adhesive material; and a multi-layered, absorbent sterile dressing affixed to the bandage. The bandage affixed with the non-adherent multi-layered absorbent sterile dressing is configured to fit within a nasal cavity.