Negative pressure wound therapy sponges that are custom-fabricated to fit a given wound to be treated, corresponding methods of creating said sponges in situ or external to a wound, and related systems for performing negative pressure wound therapy using said sponges. Exemplary sponge embodiments may have pressure-sensing capabilities.

The invention provides a wound dressing, which includes a 1 to 12 mm thick layer of absorbent non-woven fibre material between 150 and 1200 grams per square meter, which layer includes a mixture of viscose fibres and polyester fibres which more viscose than polyester, and of which the fines of the viscose is between 1.5 and 3 dtex and the fines of the polyester is between 2 and 3 dtex.

An improved abdominal hernia repair system is presented comprised of a silicone layer backed up with a knitted or woven polypropylene fabric layer, the silicone layer possessing a regular pattern of slits that permit equilibration of fluid pressure across the device. A variety of therapeutic substances can be applied to the hernia repair device to promote healing, including aloe and other medicinal preparations. A layer of water soluble or water insoluble anti-scar compound is also present, the preferred compound being Salinomycin.

An improved inguinal hernia repair system is presented that is identical to the above except it does not contain the hydrophobic silicone component.

A wound sealing powder, method of making a wound sealing powder, and method of using a wound sealing powder to reduce blood flow from a wound are provided. Specifically, the wound sealing powder utilizes a particulate powder material of an effective amount of an insoluble cation exchange material wherein the majority of the particles in the powder have particle sizes of less than approximately 48 microns.

Suture delivered patches adapted for interposition, augmentation or repair devices for use in tendon and ligament repair, including rotator cuff repair, have been developed as well as methods for their delivery using suture guided arthroscopic methods. The repair patches may be provided from suitable biocompatible materials. The patches may be delivered using anchored sutures already in use during a surgical repair including, open, minimally invasive, endoscopic, and arthroscopic repair procedures. Additionally, fixation of the suture delivered repair patch is secured along with the normal suture securing workflow of the one or more sutures used to deliver the patch.

Provided herein are methods for making foam materials and foam material products having a polyurethane foam matrix defining a plurality of pores, a hydrophilic agent retained within at least a portion of the pores for improving an absorption of the foam material, a salt retained within at least a portion of the pores in an amount sufficient to render the foam material isotonic, a surfactant retained within at least a portion of the pores in an amount sufficient to be released upon contact with a moist surface. Also provided herein are methods for making a multilayer foam by casting a second foam layer on a first foam layer substrate and compressing the second foam layer before the second layer is fully cured to form an interface layer in situ.

In the configuration of a supporter that at least partially includes a tubular cover portion which covers a part of a human body and which elastically expands and contracts, a load addition pattern portion that is adhered to at least a part of a half or more circumference in a circumferential direction on the front surface of the tubular cover portion and that can apply a load of a predetermined magnitude to the part of the human body when the part of the human body to which the tubular cover portion is fitted is moved is continuously formed of an elastic rubber material. Preferably, as the elastic rubber material, a silicone rubber material is used, and a part or the whole of the area of the load addition pattern portion is formed with a mesh-shaped portion and preferably a honeycomb shape.

The disclosure is directed to fibrous structures finished with active pharmaceutical ingredients, as well as methods of their manufacturer and use.

A wound cleaning product is described as used for sterile debridement of wounds. The wound cleaning product comprises a composite material having a foam layer and a fiber layer arranged on a surface of the foam layer. The fiber layer is at least partially thermally solidified, and the foam layer and the fiber layer are connected to one another by needling such that fibers of the fiber layer have penetrated into the foam layer and form capillary channels that extend from the fiber layer into the foam layer.

A pressure-sensing compression bandage having a plurality of pressure sensors provided to indicate the pressures applied by and/or the pressure gradient created by, the applied bandage at various locations along its length when the bandage is applied to a limb or other extremity.