A porous wound dressing for use in negative-pressure therapy is proposed. The wound dressing has an outer edge which defines a substantially oval or rectangular outer shape of the wound dressing with a major axis and a minor axis. The wound dressing has one or more incisions or perforations which together form one or more arc-shaped lines and serve for cutting the wound dressing to size in order to adapt the wound dressing to the shape and/or size of a wound. The one or more arc-shaped lines each extend asymmetrically with respect to the major axis and/or to the minor axis and each enclose, together with a portion of the outer edge, a segment of the wound dressing that is designed for separation from the wound dressing.

The present invention is directed to an absorbable hemostatic nonwoven patch that utilizes a biocompatible substrate comprised of melt-blown microfibers as webbed sheets that are layered and bonded/entangled in descending density and ascending porosity; with the substrate having a high flexibility, strength and porosity that is suitable for coating cross-linkable active molecules and ability for laparoscopic use or trocar deployment, ultimately for functional use as a highly effective hemostat in addressing problematic bleeding during both open and minimally invasive surgical procedures.

Embodiments disclosed herein are directed to the treatment of wounds using negative pressure. Some embodiments disclosed herein provide for a foam pad, which may be suitable for use in abdominal wound sites, and which may be sized in a dimensionally-independent manner. Additional embodiments provide for a wound contact layer, as well as a system for the treatment of abdominal wounds.

A breathable medical gauze patch includes at least one bandage body coupled with at least one ply of gauze or similar to, which not only helps wounds heal fast, but also prevent infections and potential complications. The at least one bandage body includes an adhesive on the underside that permits mounting about the wound site of a user/recipient. The at least one ply is disposed about a bandage aperture of the at least one bandage body. The at least one ply permits aeration therethrough to the wound site and facilitates absorption of any seepage of the wound while protecting the wound from the exterior environment. Further, the at least one ply may include multiple layers of sterilized medical grade gauze, a gel and an adhesive that allow the present invention to be efficiently and effectively applied to various deep or shallow wounds for facilitating speedy healing of the wounds.

Embodiments disclosed herein are directed to the treatment of wounds using negative pressure. Some embodiments disclosed herein provide for a foam pad, which may be suitable for use in abdominal wound sites, and which may be sized in a dimensionally-independent manner. Additional embodiments provide for a wound contact layer, as well as a system for the treatment of abdominal wounds.

A dressing for treating a tissue site with negative pressure, a sealing tape, methods of use and methods of manufacturing the sealing tape are described. The dressing includes a tissue interface configured to be positioned adjacent to the tissue site and a sealing member configured to be positioned over the tissue interface and the tissue site to form a sealed environment. The dressing also includes a sealing tape having a carrier layer having a first side and a second side, a silicone adhesive layer bonded to the first side of the carrier layer, and an acrylic adhesive layer bonded to the second side of the carrier layer. A plurality of holes extend through the silicone adhesive layer, the acrylic adhesive layer, and the carrier layer. A first release liner is coupled to silicone adhesive layer, and a second release liner is coupled to the acrylic adhesive layer.

A dressing for treating a tissue site with negative pressure may have a first layer comprising a manifold, a second layer coupled to the first layer, a third layer coupled to the second layer opposite the first layer. The second layer is formed from a first closed-cell foam and includes a plurality of apertures through the first closed-cell foam. The third layer is formed from a second closed-cell foam and includes a plurality of fluid restrictions through the second closed-cell foam that are configured to expand in response to a pressure gradient across the second closed-cell foam. The plurality of fluid restrictions are fluidly coupled with at least some of the plurality of apertures in the second layer.

A porous wound dressing for use in negative-pressure therapy is proposed. The wound dressing has an outer edge which defines a substantially oval or rectangular outer shape of the wound dressing with a major axis and a minor axis. The wound dressing has one or more incisions or perforations which together form one or more arc-shaped lines and serve for cutting the wound dressing to size in order to adapt the wound dressing to the shape and/or size of a wound. The one or more arc-shaped lines each extend asymmetrically with respect to the major axis and/or to the minor axis and each enclose, together with a portion of the outer edge, a segment of the wound dressing that is designed for separation from the wound dressing.

This technology relates to silicone-free gel adhesives with advanced skin properties for low trauma applications. These gel adhesive products provide the benefits of silicone products while improving on the major disadvantages of silicone adhesive products such as being more cost-effective and gamma sterilizable. The adhesives for this technology may be solvent acrylic, hot melt acrylics or modified block rubbers.

A wound bandage for administering light therapy is provided. The wound bandage may comprise a coated disposable flexible circuit. The disposable flexible circuit may comprise a set of plastic light-emitting diodes (LEDs). The disposable flexible circuit may be perforated and the set of LEDs may comprise at least one LED configured to emit light with a wavelength. The wound bandage may comprise a medical-grade adhesive disposed on a surface of the wound bandage. The adhesive may be configured to attach the wound bandage to a user's skin and maintain the wound bandage in a desired area. The wound bandage may comprise a socket configured to receive a connector coupled to an external control unit. The socket may transmit a control signal from the control unit to the set of LEDs and the control signal may pulse the set of LEDs at a frequency and a duty cycle.