A method for treating burns and abrasion wounds by applying a cyanoacrylate glue, using a method whereby a quantity of glue is initially applied to a flexible film of releasable material that does not adhere to the glue after it has set, and then transferring said glue to a wound site with light pressure applied through said film sufficient to control bleeding. Said application of glue under pressure will result in a thin layer of glue over the wound site that will react with the moisture present on the wound surface, thus polymerizing quickly and forming a protective coating on the wound that is flexible and sufficient to resist pathogenic penetration while simultaneously allowing the slow passage of moisture at a rate that will maintain an ideal relatively dry condition for the wound, to prevent infections that tend to develop with excessive moisture.

When configuring a skin protection sheet covering the skin disease site (including a potential skin disease site, hereinafter the same) of the user by affixing it to the inside surface of the undergarment of the user, a protective sheet main part configured in a gathered shape is provided by forming three-layered surface parts respectively formed by two fold-backs crossing in a predetermined direction at a plurality of positions in a predetermined direction, of a sheet material formed of a nonwoven fabric material, and by providing suture parts sutured in the predetermined direction by a thread material at a predetermined spacing in a direction intersecting the predetermined direction, and one, two, or more sheet affixation parts are provided on one surface of the protective sheet main part for making the protective sheet main part attachable to and removable from the inside surface of an undergarment.

A material includes a support layer comprising a woven fiber layer less than 30 mils thick. The support layer includes an elongate strap support. The support layer has a ratio of elongation to tensile strength (lb/in-width) that is less than 0.9 in a first direction and greater than 0.9 in a perpendicular second direction. The material additionally includes an adhesive layer on said support layer for adhesive attachment of said support layer to the outer skin surface of a user and a removable cover layer on said adhesive layer. Methods of use of the material and elongate strap support(s) to a human body include providing anatomical support or therapeutic effects.

A method of promoting hemostasis in the mouth or oral cavity utilizes a non-absorbent, low surface energy and highly conformable non-disruptive hemostasis material. Traditional wound packing material is highly absorbent and has large open surfaces that allow clot forming materials, such as the platelet plug to adhere to the packing material and whereupon removal, the clot is disrupted. A non-disruptive highly conformable hemostasis material does not have large open pores and therefore does not adhere to forming clots. A non-disruptive hemostasis material may consist of expanded polytetrafluoroethylene that has a pore size of no more than about 10 microns. A non-disruptive hemostasis material may comprise a thin film of material over a portion of the outside surface that is non-absorbent and thin to allow for conforming into an oral cavity, such as from a tooth extraction. A thin film may cover porous material, such as a foam, that may be elastomeric.

A barrier system is provided for use in reducing infections associated with post-operative surgical incision and/or a percutaneous medical device, such as a catheter, that is disposed within the surgical incision. Such a barrier system may include: a barrier device having a skin-contacting surface and a catheter-receiving surface; and an adhesive composition configured for adhering to skin, the barrier device, and/or the catheter so as to form a barrier at or adjacent to an incision in the skin where the catheter is percutaneously inserted through the skin. A tensioning anchor and associated system of two or more tensioning anchors is provided for post-operative wound closure. A method for applying and removing the barrier device and tensioning anchors is also provided.

A dome bandage is a reusable device for covering wounds, optical viewing, and protecting from external objects while wound heals. In one form, the dome bandage is composed of clear transparent synthetic ultraviolet resistant rigid shatter proof reusable shell dome with size and shape in degrees from circular to ellipticity; and from squareness to oblongness mold; with slits on the flange for attaching porous non-adhesive ribbon tape to rap around the uninjured part of the human anatomy.

Systems and methods can promote wound healing, including a wound dressing having a wound-facing surface and a second surface. The wound-facing surface can be configured to contact a wound of a patient. There can also be at least one conduit having an interior lumen operably connectable to the second surface of the wound dressing, a central window configured to allow air flow from the interior lumen of the conduit to the wound-facing surface of the wound dressing, and a flexible wrap operably connectable to the conduit.

An apparatus suspends a post-amputation residuum protection device for a below the knee amputation. The suspending apparatus comprises an elongated arcuate first shell defining an open interior channel. The first shell is adapted to receive at least a portion of the residuum and the residuum protection device into the interior channel. A flexible second shell includes a circumferential wedge extending radially inwardly from a portion of an inner surface. The second shell is configured to be received within the first shell and adapted to cover the residuum adjacent to the knee. The wedge is adapted to bear against the residuum above the medial femoral condyle such that the wedge is received in the supracondylar space for suspending the residuum protection device.

A barrier system is provided for use in reducing infections associated with post-operative surgical incision and/or a percutaneous medical device, such as a catheter, that is disposed within the surgical incision. Such a barrier system may include: a barrier device having a skin-contacting surface and a catheter-receiving surface; and an adhesive composition configured for adhering to skin, the barrier device, and/or the catheter so as to form a barrier at or adjacent to an incision in the skin where the catheter is percutaneously inserted through the skin. A tensioning anchor and associated system of two or more tensioning anchors is provided for post-operative wound closure. A method for applying and removing the barrier device and tensioning anchors is also provided.

A bandage with a center that elevates over an open wound or desired portion of skin to be covered which forms a dome that has tiny vent holes to allow air inside. The dome allows fresh air to the wound while it is still protected from harmful bacteria, infections, virus' or disease.