A bandage comprising a base substrate and a mechanical coupling system. The base substrate has an inner surface and an outer surface and a central region positionable over a wound. The mechanical coupling system comprising at least two mechanical coupling members spaced apart from each other and spaced apart from the central region. At least one of the at least two mechanical coupling members having a base and a plurality of gripping structures. The plurality of gripping structures each extend from the lower surface of the base, and have a base configuration and an upstanding structure. The upstanding structure curves so as to terminate at a tip. The tip defining a tip axis, wherein the tip axis is between +10 and 10 of an axis extending from the tip that is substantially parallel to the lower surface of the base.

The present invention relates to methods and devices for skin tightening after incising or excising tissue portions from a subject. Exemplary methods and devices include tunable dressings having an adhesive layer and a regulatable layer or an un-stretched layer that responds to one or more external stimuli to contract or expand the dressing, where the contraction or expansion can be uniform or non-uniform.

Wounds and temporary appliances can be protected against liquid contamination using a prophylactic dressing. The dressing includes a liquid resistant sheet and disposed thereon a first liquid barrier/adhesive strip and a second liquid barrier/adhesive strip wherein the first and second liquid barrier/adhesive strips are concentric; located at or near the periphery of the liquid resistant sheet; and are separated from one another by a gap. Adsorbent's and liquid indicators can be employed within the gap to add further functionality to the dressing. Also disclosed herein is a support useful for stabilizing leads to transcutaneous or percutaneous devices.

A viscoelastic wound closure dressing. The dressing can include a viscoelastic backing having a first major surface configured to face skin when in use, a first end, a second end, and a middle section located between the first end and the second end. The wound closure dressing can further include a skin-contact adhesive on the first major surface of the viscoelastic backing adjacent the first end and the second end. A majority of the first major surface of the middle section can be free of the skin-contact adhesive. The viscoelastic backing can recover, at room temperature: (i) no more than 40% of its deformation after 10 seconds, after being strained to 50% elongation for 30 minutes, and (ii) at least 70% of its deformation after 48 hours, after being strained to 50% elongation for 30 minutes.

A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.

A nonpermeable enclosure formed from a clear, waterproof fabric, has a cover ridge for insertion into a channel so as to produce a barrier against moisture and contaminants, and is attached to a closure band for securing the nonpermeable enclosure over a wearer's hand.

A protective umbilical cord cover having a containment portion being adapted to protect an umbilical cord of an infant and also an attachment mechanism being adapted to releasably attach the containment portion against the infant. The protective umbilical cord cover may also include an umbilical cord cover material that is constructed to form the containment portion, wherein the umbilical cord cover material is liquid impermeable in an inward-flow direction. The protective umbilical cord cover may also include an umbilical cord cover material that is constructed to form the containment portion, wherein the umbilical cord cover material is vapor permeable in an outward-flow direction. The protective umbilical cord cover may also include an umbilical cord cover material that is constructed to form the containment portion, wherein the umbilical cord cover material is vapor permeable in an outward-flow direction.

A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.

Devices, bandages, kits and methods are described that can control or regulate the mechanical environment of a wound to ameliorate scar and/or keloid formation. The mechanical environment of a wound includes stress, strain, and any combination of stress and strain. The control of a wound's mechanical environment can be active, passive, dynamic, or static. The devices are configured to be removably secured to a skin surface in proximity to the wound site and shield the wound from endogenous and/or exogenous stress.

A wound protection device can include a frame having a plurality of first members and a plurality of second members. The first members can be spaced relative to each other. The second members can be spaced relative to each other and can be coupled to the first members. The first members and the second members can define a plurality of a gaps through which a fluid can enter the frame. The frame can be configured to circumscribe a wound.