An adhesive convertible tissue stabilizer is provided which can be applied preoperatively to a patient to retract tissue to facilitate a medical/surgical procedure. As a perioperative device, the convertible device accepts most, if not all, surgical preparations, enabling the creation of a sterile field. At the completion of the procedure, the convertible device is converted from a perioperative device to a post-operative device by removal of a layer of the convertible device.

A method for accurately, rapidly and consistently cutting an opening in drape material for negative pressure wound therapy (NPWT) uses a cutting device that includes a plurality of cutting members that can extend from a bottom surface of the cutting device. A cover may fit over the bottom to protect the cutting members. The cutting members may be positioned to define a cut-out shape having dimensions designed for use with a NPWT system. An adhesive material may be formed on the bottom surface of the cutting device, inside of the cut-out shape defined by the cutting members. In use, the user presses the cutting tool onto the drape to cause the cutting members to cut into the drape and the adhesive to stick to the drape. When the user lifts the device, the drape, cut to the correct size and shape, is removed from the foam dressing covering the wound.

A vacuum sponge system, comprising: a sponge having an outer surface, a proximal end and a distal end, spaced from the proximal end in an axial direction of the sponge; a drainage tube disposed partially in the sponge, and is in fluid communication with the sponge; the drainage tube is connectable with a vacuum pump such that a pressure is applicable to the outer surface of the sponge; and a delivery member having an outer surface and extending in an axial direction of the sponge and adapted to establish a fluid communication between a region from the distal end of the sponge and region from the proximal end of the sponge. The pressure provided by the pump via the drainage tube is applied to a vicinity of the outer surface of the delivery member and the outer surface of the sponge. The delivery member is disposed partially radially outside of the sponge.

Disclosed herein are systems and methods for safe operation of a wound treatment apparatus with electronic components integrated on or within a wound dressing. In some embodiments, the electronic components include a power source, an isolation circuit, a controller, a capacitor, and a negative pressure source. The isolation circuit provides multiple activation states with at least one state preventing application of power to the other electronic components capable of storing electrical energy, thereby providing a safe operation of the apparatus. For example, sterilization of the apparatus can be performed safely.

The wound therapy apparatus may include a wound interface sealingly securable to the skin surface around a wound bed to encloses the wound bed within an enclosed space that is fluid-tight. The wound interface may be sufficiently deformation resistant to distend at least a portion of the wound bed into the enclosed space when pressure p.sub.0 within the enclosed space is less than ambient pressure p.sub.amb. Fluid may be communicated with the enclosed space when the wound interface is sealingly secured to the skin surface in order to vary a pressure p.sub.0 within the enclosed space periodically over the pressure range p.sub.min≤p.sub.0≤p.sub.max. The variation of the pressure p.sub.0 may distend the wound bed into communication with a pad received within the enclosed space and decreases the wound bed contact with the pad. Related methods of use of the wound therapy apparatus are also disclosed.

Disclosed embodiments relate to apparatuses and methods for wound treatment. In certain embodiments, a negative pressure wound therapy apparatus can include a wound dressing comprising an absorbent layer comprising a plurality of portions of absorbent material that can be physically separate from each other. In some embodiments, a wound treatment apparatus can include an absorbent layer comprising a compressed portion configured to impede the flow of fluid therethrough. In some embodiments, a wound treatment apparatus can include an absorbent layer and spacer layer positioned side by side.

The present disclosure relates to wound bandages. More specifically, the present disclosure describes a vacuum sealed bandage having a film layer that is manipulable into a wound by way of negative pressure imparted by a removable medical syringe. The vacuum sealed bandage of the present disclosure does not have a vacuum pump, does not constantly apply negative pressure to the wound through an electro-mechanical device or vacuum pump, and/or does not have chords or tubes positioned to opposite sides of the film layer or extending from one side of the film layer to another side of a film layer where the chord or tube is positioned between the film and the wound.

A negative pressure device for applying to skin is configured to define a sealed enclosed three-dimensional space when at least a portion of the device is sealed against the skin. The device includes a body including at least one expandable segment that is configured to expand after the device has been sealed against the skin.

An absorbent component for a wound dressing comprises a stitch bonded nonwoven substrate wherein the nonwoven substrate is stitch bonded with an elastomeric yarn and wherein the nonwoven substrate comprises a superabsorbent material and/or a gelling material. Also disclosed is a method of manufacturing the absorbent component, a wound dressing or a negative pressure apparatus comprising the absorbent component and a method of treating a wound using said wound dressing or negative pressure apparatus comprising the absorbent component.

A negative pressure wound therapy system can include a housing and a source of negative pressure enclosed by the housing configured to aspirate fluid from a wound covered by a wound dressing. The system can have one or more visual indicators visible at the exterior surface of the housing, configured to indicate status of the system to a user. The system can also have electronic circuitry enclosed by the housing, the electronic circuitry configured to automatically, or in response to a request from the user, transition the system between at least a first operational state and a second operational state, wherein in the second operational state the one or more visual indicators are configured to not emit any light or to emit light at one or more wavelengths that are not visible to naked human eye.