A closing dressing bolster and assembly for use with a system for treating a linear wound on a patient includes a bolster body formed from a flexible closing bolster material having closing members that are operable to develop an inward closing force when the closing dressing bolster is placed under reduced pressure. In one aspect, when the closing dressing bolster is under reduced pressure, the system, dressing, or assembly develops an inward force realized at the linear wound and a compression force. A wicking-material holder and wicking material may be used as well. The member components may all be see-through to allow visual inspection of the wound without requiring removal of the dressing.

A packaged kit of parts is provided for use with a selectively configurable wound dressing. The kit includes a piercing tool configured to pierce a covering layer of the wound dressing to produce an aperture therein and thereby configure the wound dressing for use in a pressure gradient wound therapy system. The kit may also include a) packaging indicating that the piercing tool is configured to pierce a covering layer of a wound dressing; (b) instructions instructing a user as to how to use the piecing tool; (c) one or more selectively configurable wound dressings; (d) a source of non-atmospheric pressure; (e) a port to connect the wound dressing to a source of non-atmospheric pressure; or (f) tubing for connection between a wound dressing and a source of non-atmospheric pressure. The kit is arranged within a sealed package.

The methods, procedures, kits, and devices described herein assist with the healing process of tissue that was previously or simultaneously treated for a therapeutic or cosmetic effect. The methods, procedures, kits, and devices described herein can also provide temporary simulated results of a cosmetic procedure to allow for visual assessment to select the type of procedure or for treatment planning in advance of the surgical procedure.

Described is a negative wound therapy (NPWT) dressing that includes a backing layer and an adhesive skin contact layer, the adhesive skin contact layer being configured to detachably adhere the dressing to a dermal surface, wherein the backing layer includes a coupling member. The coupling member includes a tubing configured to connect the dressing to a negative pressure source and to a remote fluid collector.

A dressing may comprise a manifold having a first planar surface and a second planar surface opposite the first planar surface, and a first layer adjacent to the first planar surface and a second layer adjacent to the second planar surface. The first layer and the second layer may be laminated to the first planar surface and the second planar surface, respectively. Pressure-responsive fluid restrictions through at least one of the first layer and the second layer may be adjacent to the manifold. The first layer and the second layer may also form a sleeve or an envelope around the manifold in some embodiments. At least one of the first layer and the second layer may be configured to be disposed between the manifold and a tissue site in use. In some examples, the dressing may have a smooth or matte surface configured to contact a tissue site.

A dressing including a film which is impermeable to fluids and permeable to water vapor, and the entire surface of which is covered by a perforated reinforcement coated with a medically acceptable adhesive which is the same or different on each of the faces thereof, the face opposite to the face in contact with the impermeable film of an adhesive being partially covered by an absorbent pad, The dressing further includes a layer for distributing the fluids which is positioned between the impermeable film and the perforated reinforcement.

A dressing for a wound includes a drape, an absorbent core, and a wicking member. The drape can be configured to sealingly couple with a patient's skin surrounding the wound. The drape may enclose an inner volume of the dressing. The absorbent core layer may be positioned within the inner volume of the dressing. The wicking member is positioned within the inner volume, wherein the wicking member extends from an underside of the absorbent core layer to the drape. The indicator may be configured to fluidly couple with the wicking member through the drape and receive fluid from the wicking member. The indicator may be configured to provide a visual wound status indication in response to receiving fluid from the wound through the wicking member.

Embodiments disclosed herein are directed to negative pressure treatment systems and wound dressing systems, apparatuses, and methods that may be used for the treatment of wounds. In particular, some embodiments are directed to improved wound dressings comprising an obscuring layer that may hide fluid contained therein. Some embodiments may further comprise one or more viewing windows disposed therethrough so as to enable monitoring or examination of fluids contained therein.

A dressing for treating a tissue site with negative pressure may comprise a cover having an adhesive, a manifold, a perforated polymer film, and a perforated silicone gel having a treatment aperture. The cover, the manifold, the perforated polymer film, and the perforated silicone gel may be assembled in a stacked relationship with the cover and the perforated silicone gel enclosing the manifold. The perforated polymer film may be at least partially exposed through the treatment aperture, and at least some of the adhesive may be exposed through the perforated silicone around the treatment aperture.

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.