A compression device for compressing an area of tissue surrounding a tissue opening to close the tissue opening. The device includes a compression support frame having an outer peripheral edge forming an arc whose central angle is less than 180° and greater than 45°. The device also includes a compression support and a tension member. The compression support is mounted on the compression support frame, and the tension member is selectively slidable in relation to the compression support.

A wound closure device includes an elastic substrate and a plurality of microstructure arrays coupled to the elastic substrate via an adhesive layer. The device is long enough or wide enough to treat large wounds with the plurality of microstructure arrays distributed along a length of the wound.

Disclosed is a two-component medical device useful for closing a wound or incision. The two-component medical device includes first and second adhesive-backed anchoring members having wound edges. A first and a second release liner protect the first adhesive-backed surface of the first adhesive-backed anchoring member. A first and a second release liner also protects the second adhesive-backed anchoring member. Each of the first and second release liners include a tab portion for removal of the associated first or second release liner.

A wound healing device and method that greatly reduces the risk of infection of an incision or wound by removing fluid from the subcutaneous skin layers. The wound healing device includes a first portion that is positioned external of, and on top of, the wound. At least one strip, cord, finger, member is in fluid communication at one end with the first portion while the second free end of the at least one strip, cord, finger, member is pushed down into the wound, in between the sutures or staples of a closed incision. Both the first portion and the at least one strip comprise fluid absorbable material for absorbing the wound fluid. The device remains in place for approximately 1-3 days after which it is removed. Upon removal, natural temporary “type of fistulae” are formed in the subcutaneous skin layers to continue draining wound fluids upward for another 1-2 days.

An adhesion promotion device is disclosed, which is capable of reducing risk factors of an anastomotic leakage after surgery. The adhesion promotion device has a main body portion disposed between biological organs serving as a joint object. The main body portion has a first region and a second region formed along an outer edge of the first region. The second region includes an adhesion promotion portion that promotes adhesion of a biological tissue. The first region includes a holding portion having a holding force with respect to the biological tissue which is stronger than that of the adhesion promotion portion.

Occlusive tissue dressings and methods including an elastomeric drape and a liquid component, at least partially cross-linked at least after one of drying and curing, suitable for application at a dressing-to-skin interface in order to create a substantially air-tight seal. The same or a different liquid component may be applied by a user at a tube-to-dressing interface in order to create a similar air-tight seal around the tube, if not occlusively sealed during its manufacture.

Devices, tools, systems, kits and methods for closing a tissue opening non-invasively are presented. The devices include a tissue closure device that reliably induces eversion of tissue edges that define a tissue opening.

A wound closure system includes a device having a first main body and a second main body. Each of the first main body and the second main body has an adhesive backing. The first main body is coupled to the second main body by an adjustable connector. The adjustable connector is permitted to move in a single direction. In the event of an injury, the first and second main bodies are placed on opposite sides of a wound and are then pulled together, thereby sealing the wound.

A wound closure system includes a device having a first main body and a second main body. Each of the first main body and the second main body has an adhesive backing. The first main body is coupled to the second main body by an adjustable connector. The adjustable connector is permitted to move in a single direction. In the event of an injury, the first and second main bodies are placed on opposite sides of a wound and are then pulled together, thereby sealing the wound.

Disclosed is a two-component device for closing a wound or incision. The two-component device includes a first elongated component and a second elongated component, wherein at least one of the first elongated component or the second elongated component comprises a plurality of lateral translation elements.