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.

An apparatus that includes a mask is provided, the mask including one or more fixation anchoring devices, each configured to anchor to an at least one body part within a user, wherein the at least one body part includes at least a portion of one or more of an oral, nasal, pharyngeal, and a respiratory airway; one or more skin covers, each capable of covering at least a portion of the user's face, wherein one or more of the fixation anchoring devices are connected to one or more skin covers; one or more conduits, each connected to at least a portion of one of the skin covers, wherein one or more of a gas, solid, liquid, and gel are transmitted through each of the conduits; and one or more sealing pads, each connected to at least one of one of the skin coverings and one of the fixation anchoring devices.

Composite wound dressings including an activated carbon material, a barrier material layer, a liquid-absorbing material layer and an outer liquid-impermeable layer are disclosed herein. The composite wound dressings include a bond substantially bonding a portion of the liquid-impermeable outer layer and the barrier material layer to the activated carbon containing layer, the bond forming a sealed pouch of un-bonded layer of the composite and encapsulating the liquid-absorbing layer. Methods for manufacturing and using such composite wound dressings to effectuate healing of wounds on humans or other animals are described herein.

A surgical sponge including a sponge material configured an elongate sponge having multiple compressed layers and a flattened shape characterized by a generally flat upper surface, a generally flat lower surface, with the sponge having a thickness that is substantially less than a width of the sponge, one reduced dimension end of the elongate sponge having an end length and reducing in dimension distally along the end length; stitches along the length of the sponge to compress the sponge material and maintain the layers in compression to maintain the flattened shape of the sponge; and a length of stitch material extending from the reduced dimension end to provide a structure that is engageable for use in positioning or removal of the sponge during a surgical procedure.

Implantable medical constructs formed by winding using winding support structures that can be flexible and can be integrated into the medical construct with biocompatible fiber(s) and/or yarn(s) and at least one continuous length collagen fiber. The implantable medical construct can include open suture anchor apertures formed using posts during a winding sequence.

The specification describes membranes, formulations, methods of manufacture, and methods to develop formulations and membranes that have desired physical properties. The membranes and formulations are biodegradable, in conditions like domestic and commercial compost systems. The formulations and membranes may also be flexible and have desired physical properties such as melting point and flexibility.

Disclosed are compositions that comprise an organic electrochemical mediator and a gasotransmitter salt which converts into a gasotransmitter via electron transfer. Also disclosed are bandages and wound dressings comprising the subject gasotransmitters, and methods of making a gasotransmitters, comprising exposing the compositions to a voltage sufficient to reduce the water soluble organic mediator. Further disclosed are methods of treating a variety of trauma and disease states by applying a therapeutically effective amount of at least one gasotransmitter thereto, and methods of generating an effective dose of the gasotransmitter generated from electrolytic reaction involving the gasotransmitter-generating compositions.

A wound dressing includes an absorbent core including a top surface and a bottom surface containing a superabsorbent substance, a facing layer including folded sections folded towards the top surface of the absorbent core, the facing layer entirely covering the bottom surface of the absorbent core, a backing layer, and a contact layer including folded sections covering parts of the folded sections of the facing layer, the contact layer folded to cover an entire area of the facing layer covering the bottom surface of the absorbent core and the contact layer is configured to be brought into contact with a wound. The facing layer and the backing layer form a pouch in which the absorbent core is located. The folded sections of the facing layer and the backing layer are joined together. The folded sections of the contact layer and the facing layer or the backing layer are joined together.

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.

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.