The present invention relates to dressings such as bandages or tapes having improved extensibility and conformability to human skin and joints.

The present invention generally relates to dressings such as bandages or tapes having improved extensibility and conformability to human skin and joints.

The present invention generally relates to dressings such as bandages or tapes having improved extensibility and conformability to human skin and joints.

Cushioning articles include a layer with a plurality of cuts arrayed in a pattern. The cuts are gaps and the gaps do not form apertures allowing one to see through the layer when the layer is in an unstressed state, but in a stressed state, at least some of the cuts become gaps that are perforations through the layer. In the stressed state the layer expands to form the cushioning article. The cushioning article may be a multi-layer article with another layer that is contacted to the stressed layer in the stressed state to hold the layer in a stressed state.

Methods and products for protecting tissue of a patient during a surgical procedure that involve making an incision in the tissue and retracting the tissue to make a larger opening, wherein the methods and products use a water-absorbing stress-distributing layer.

The compressive bandage includes an elastic cap to fit over the patient's head wound and head. The cap is impervious to fluid and has a fluid pervious inboard sleeve pocket. An absorbent pad placed in the sleeve since the sleeve and the cap expands. The loaded bandage is placed on the head wound. The pocket patch is a micro fiber, polyester fabric, preferably NIKE DRY FIT material. The head wound is stanched by placing the over the head wound. After the first use and after removal from the wounded head, the first pad is withdrawn from the pocket, a second pad in inserted and the compressive bandage is again placed on the head wound. After the first use or the second use, the bandage can be washed and sterilized.

A see-through dressing assembly is presented for use with a reduced-pressure system for treating a wound on a patient using reduced pressure that allows visual observation of the wound during treatment. The dressing assembly includes a bolster for providing a directed force when under reduced pressure, a sealing member for covering the bolster and providing a seal over the bolster and a patient's epidermis, and wherein the bolster and sealing member are formed from see-through materials sufficient to allow perception of color from a point external to the system. Other systems, dressings, and methods are presented.

A method of manufacturing a reduced-pressure abdominal treatment system for treating an open abdominal cavity is provided. In some embodiments, the reduced-pressure abdominal treatment system has an open-cavity treatment device for providing reduced-pressure treatment to an abdominal cavity; a deep-tissue closure device for applying a closing force on a deep-tissue wound; and a surface-wound closure subsystem for providing a closing force on a surface wound. The method of manufacturing may also include providing a reduced-pressure supply subsystem. A method of treatment using a reduced-pressure abdominal treatment system is also disclosed.

A compression device for applying compression to a body part of a user. The compression device has a sleeve with two lateral side regions and a central region in-between. The central region of the sleeve comprises a main material having elasticity in at least a transverse direction. A maximum elongation in the transverse direction is from 5% up to and including 30% under a load of 10 N per cm width and a difference quotient of tension in the transverse direction from 20% elongation to 25% elongation equal to or greater that 0.6 N per cm width per percent elongation. The device further includes a releasable closure system configured and arranged relative to the sleeve, such that, in use, upon closure of the closure system the sleeve is restrained and tightened about the body part of the user.

A wound care device that can be effectively attached to a wide range of wound locations without the use of any adhesives, can apply controlled, consistent pressure to the wound, and can be configured to allow the clinician to see relevant areas of the patient's body is disclosed. The wound care device includes a contact pad connected with a securing strap. The securing strap includes an inelastic strap segment and an elastic strap segment. The elastic strap segment is coupled with an attachment segment, which attaches to the inelastic strap segment and cooperates with the elastic strap segment to compress the contact pad to the wound.