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.

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.

A dressing includes a hydrophilic foam layer having a longitudinal central axis configured to overlay the incision, a drape coupled to an outwardly-facing side of the hydrophilic foam layer, a first row of superabsorbent material positioned on the outwardly-facing side of the hydrophilic foam layer, and a second row of superabsorbent material positioned on the outwardly-facing side of the hydrophilic foam layer. The first row and the second row are spaced laterally apart from, and on opposite sides of, the longitudinal central axis. The drape includes a first window aligned with the first row and a second window aligned with the second row. The first window and the second window include a film, different from the drape, configured to facilitate evaporation therethrough.

An apparatus, system, and method for treating an incisional wound having incisional walls. The apparatus includes a conduit having a first end for receiving reduced pressure and a second end. The apparatus further includes a scaffold. The scaffold has opposing surfaces for positioning adjacent the incisional walls and is fluidly coupled to the second end of the conduit for receiving the reduced pressure. The scaffold is generally elongated in shape and has a thickness between the opposing surfaces that is sufficiently thin for positioning within the incisional wound. The apparatus further includes an internal manifold that has a primary flow channel extending generally longitudinally within the scaffold and between the opposing surfaces of the scaffold. The internal manifold is fluidly coupled to the second end of the conduit. The application of the reduced pressure through the scaffold and the internal manifold induces tissue apposition between the incisional walls.

Problem

To provide a skin closure tape or a reinforcing tape used after skin-suture.

Solution

A skin closure tape or a reinforcing tape used after skin-suture that includes a backing made of at least a nonwoven fabric and an adhesion layer disposed on a surface on one side of the backing. A plurality of resin stripes are disposed on a surface on another side or/and the surface on the one side of the backing. The plurality of the resin stripes extend in a longitudinal direction of the backing.

An apparatus, system, and method for treating an incisional wound having incisional walls is disclosed. The apparatus includes a conduit having a first end for receiving reduced pressure and a second end. The apparatus further includes a scaffold. The scaffold has opposing surfaces for positioning adjacent the incisional walls and is fluidly coupled to the second end of the conduit for receiving the reduced pressure. The scaffold is generally elongated in shape and has a thickness between the opposing surfaces that is sufficiently thin for positioning within the incisional wound. The apparatus further includes an internal manifold that has a primary flow channel extending generally longitudinally within the scaffold and between the opposing surfaces of the scaffold. The internal manifold is fluidly coupled to the second end of the conduit. The application of the reduced pressure through the scaffold and the internal manifold induces tissue apposition between the incisional walls.

An apparatus, system, and method for treating an incisional wound having incisional walls is disclosed. The apparatus includes a conduit having a first end for receiving reduced pressure and a second end. The apparatus further includes a scaffold. The scaffold has opposing surfaces for positioning adjacent the incisional walls and is fluidly coupled to the second end of the conduit for receiving the reduced pressure. The scaffold is generally elongated in shape and has a thickness between the opposing surfaces that is sufficiently thin for positioning within the incisional wound. The apparatus further includes an internal manifold that has a primary flow channel extending generally longitudinally within the scaffold and between the opposing surfaces of the scaffold. The internal manifold is fluidly coupled to the second end of the conduit. The application of the reduced pressure through the scaffold and the internal manifold induces tissue apposition between the incisional walls.

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 outward for another 1-2 days.

A laceration closure reinforcement device includes a medical mesh impregnated with a viscous monomeric medical adhesive that completely coats a first surface and a second surface of the medical mesh. A method of reinforcing a prepared laceration includes removing the device from protective packaging; removing a first release film from the medical mesh; applying the first surface of the mesh to a prepared laceration; massaging a second release film; and removing the release film from the second surface. The mesh completely contacts all portions of the laceration, the closure strips, and a region of surrounding skin. This flexible, strong laceration repair is especially important on curvilinear surfaces where dehiscent shear and tensile forces, that occur in healing repaired minor and complex traumatic lacerations, are intensified. It increases the reliability of a laceration repair with monomeric adhesive by insuring maximum strength of the repair.

The present invention resides in a sutureless wound closure device for external use. The device comprises a base layer for fixing the device to skin and an upper layer. The base layer includes an aperture therein. The upper layer has a first end anchored to the base layer and a second, opposite end that includes fixing means to attach the end to the base layer and close the aperture in the base layer.