Abstract: A drug delivery system that includes an elongated inert support and at least two reservoirs containing a pharmaceutically active ingredient. The inert support has a number of wall segments that define at least two compartments arranged for accommodating the at least two reservoirs. The inert support is made of a material which prevents migration or diffusion of the active ingredient from one reservoir into the other or into the support. Since the drug delivery system is divided into compartments, one for each reservoir containing an active ingredient, the release rates of each active ingredient can be independently controlled or adjusted. This is due to the fact that there is no interaction between the active ingredients, and accordingly the active ingredients will not influence each other physically or chemically.

Abstract: Tapes and methods including an unbacked construction of at least one liquid layer adhesive that has been at least one of dried and cured. Occlusive tissue dressings, tapes and methods including an elastomeric drape and, for backed drapes and some unbacked drapes, a liquid component, at least partially cross-linked at least after one of drying and curing, suitable for application at a dressing-to-skin interface in order to create a substantially air-tight seal. The same or a different liquid component may be applied by a user at a tube-to-dressing interface of an elastomeric drape to create a similar air-tight seal around the tube, if not occlusively sealed during its manufacture. Featured are unbacked tapes, a drape with liquid sealant component, a liquid layered drape with liquid sealant component, and a liquid layered drape.

Abstract: A knee orthosis is provided. In described embodiments, the knee orthosis is designed to follow a natural movement of a wearer's knee along an asymmetric helicoidal axis of rotation. In some embodiments, the knee orthosis has hinges with shells having displacing geometric centers which do not coincide. In some embodiments, the knee orthosis is made of femoral and tibial hinges manufactured as single integral pieces. In some embodiments, the orthosis is configured to realign the wearer's knee in a frontal plane. Corresponding methods for designing and manufacturing a custom knee orthosis are also provided.

Abstract: An adjustable orthostatic intolerance garment formed of a knitted spandex powernet construction in order to provide compression when on the leg, and including legs and a torso portion that extends upwardly into the abdominal area below the pectoral muscles; and a respective pair of elongate panels that are retained in place by attaching elements, and that are introduced into or removed from the garment to increase or reduce compression on the wearer's body as desired.

Abstract: A compression bandage in the form of a knit obtained with warp knit technology, formed of synthetic yarns and composed of two textile surfaces having the same or different textile structure, linked together by spacer threads, each surface has elastic yarns, and the spacer threads of the knit are multifilaments. The knit has longitudinal elongation measured as per standard EN 14704-1 of between 30 and 160% and threshold shear stress equal to or higher than 2800 Pa and/or conformability equal to or lower than 65 mm.

Abstract: A dressing is described having a backing layer, an (absorbent) pad, an adhesive coating and a release liner. The release liner is releasably attached to the adhesive coating. The release liner is configured to stiffen up and protect protrusions and/or border portions of the dressing that may otherwise be wrinkled, folded, kinked or otherwise damaged or impaired prior to (transportation or storage) or during application at the point-of-use. The dressing can be used for wound treatment. The dressing can prevent shearing and/or friction from causing (deep tissue) skin damage.

Abstract: One or more embodiments include antimicrobial bandages with nanostructures, formation thereof, and usage thereof to facilitate wound healing. In one embodiment, a bandage apparatus that facilitates healing a wound is provided. The bandage apparatus includes a substrate having an attachment mechanism that facilitates removably attaching the substrate to a part of a body having the wound. The bandage apparatus also includes a nanostructure film provided on a surface of the substrate and configured to contact the wound when the substrate is attached to the part of the body having the wound, wherein the nanostructure film includes a plurality of nanostructures.

Abstract: An incontinence clamp is provided. The incontinence clamp includes an upper clamp arm and a lower clamp arm. Each of the upper and lower clamp arms include a first end, a second end, an inner surface and an outer surface. The inner surfaces face each other. A hinge pivotally connects the first ends of the upper and lower clamp arms together. An upper guide is coupled to the inner surface of the upper clamp arm and a lower guide is coupled to the inner surface of the lower clamp arm. A connector releasably connects the second ends of the upper clamp arm and the lower clamp arm together.

Abstract: A portable spinal decompression device includes a top (thoracic) adjustable belt and bottom (lumbar) adjustable belt with a plurality of traction devices attached at set anchor points for applying traction forces to a body to facilitate spinal disc decompression and alleviate pain of users with spinal disorders. The portable device that fits various shapes and body sizes can be operated by a user without additional assistance and can be used while the individual is in numerous positions during his or her daily routine.

Abstract: A surgical drape is disclosed herein that is to be used for medical procedures in order to ensure sterile portions are not contaminated. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a u-shaped opening, at least one sleeve, and at least one flap on its proximal end. The at least one sleeve and the at least one flap extend outwardly from a top surface of the drape. The at least one flap includes adhesive components on one side that allow the at least one flap to be folded back on to itself to provide additional protective barrier from contamination.

Abstract: A wound dressing (10) for covering a wound, including an absorbent layer (12) with an upper side (14) and a lower side (18), the upper side being coated with a protective layer (16). At least one cut (26) and at least one perforated dividing line (28) is incorporated into the absorbent layer (12) to form at least one segment (30, 32, 34, 36), which can be separated from the absorbent layer (12) without tools. An adhesive section (40) originates from the protective layer (16) for covering the at least one cut (26) and the at least one perforated dividing line (28).

Abstract: A medical dressing for application to a surface of a human body is described. The medical dressing has a first direction (x) of extension and a second direction (y) of extension being perpendicular to the first direction (x) of extension. The medical dressing has at least a first and a second anisotropic layer having anisotropic stiffness, wherein the stiffness of each one of the first and the second anisotropic layer is higher in the second direction (y) of extension than in the first direction (x) of extension.

Abstract: A surgical drape assembly can include a surgical drape; and a cinch assembly affixed to the surgical drape. The cinch assembly can include a folding mechanism having a plurality of links and at least two hinge joints respectively connecting respective adjacent links of the plurality of links. The plurality of links can be foldable relative to one another about the at least two hinge joints between an unfolded configuration and a folded configuration. A first portion of the surgical drape is in an extended configuration in the unfolded configuration with a portion of the drape being in a gathered configuration in the folded configuration of the plurality of links.

Abstract: A surgical drape is configured for covering a patient and an ultrasonography probe during surgical treatment of the patient. The surgical drape may include a first portion that includes a canopy portion. The canopy portion can be sized and shaped to at least partially cover a mechanical arm coupled to the ultrasonography probe and a proximal portion of the ultrasonography probe, and the canopy portion can be configured to move with the proximal portion of the ultrasonography probe when the ultrasonography probe is supported by the mechanical arm. A second portion can be coupled to the first portion, in which the second portion is sized and shaped to cover at least a portion of a torso of the patient.

Abstract: An exoskeletal orthosis includes a proximal cuff including a hinge along an upper edge of the cuff; an ankle section/footplate; and at least one posterior strut connecting the proximal cuff to the ankle section and foot plate.

Abstract: Described herein are systems and devices for providing an orthopedic walking brace having a housing and a sole with a curved distal surface. The housing is configured to encompass and immobilize a patient's ankle against flexion. The distal surface of the sole has a posterior region, a mid region, and an anterior region. The posterior region is configured to lie under a heel portion of the patient's foot and has a first anterior-posterior (AP) curvature that increases from a posterior side of the posterior region toward a middle portion of the posterior region and decreases from the middle portion of the posterior region toward the mid region. The mid region is configured to lie under a center portion of the patient's foot. The anterior region is configured to lie under an anterior metatarsal and toe portion of the patient's foot and has a second AP curvature.

Abstract: Spinal weighting devices has pairs of adjustable padding on supporting frames for making contacting selected portions of the core or trunk of a patient and includes an extending armature for applying force to urge at least one of the contacting pads to adjust the spine and/or cause the selective strengthening of muscles or muscles groups to correct scoliosis. The opposing padding members are disposed at oblique angles to correct spinal rotation as well as lateral curvature.

Abstract: A cervical collar has a height adjustment system between upper and lower parts forming an anterior component for increasing height of the anterior component inclusive of a tracheal opening. The anterior component is arranged to permit the use of known mandibular and occipital supports in the cervical collar to maintain their functionality, comfort and fit, including their anatomical contours and connection to the height adjusted anterior component.

Abstract: A surgical draping system includes an under-draping, an over-draping, and a connecting draping connected by the under-draping and the over-draping. The surgical draping system is used to establish and maintain a surgical corridor to a surgical site or sites on a patient supported by a surgical table. The surgical draping system can accommodate rotation of the patient on the surgical table, such that the sterile surgical corridor is maintained even during such rotation. The sterile surgical corridor extends through an aperture formed in the over-draping, through an enclosed passageway formed through the connecting draping, and through an aperture formed in the under-draping.

Abstract: A dressing for applying pressure to a patient target site is provided. The dressing includes an elastic spacer longitudinally extending between first and second substrates. The elastic spacer is configured to be selectively moved between the first length and a second length. The second length is longer than the first length. A triggering element, when present, selectively maintains the elastic spacer at the second length and selectively prevents the elastic spacer from moving toward the first length. Portions of the triggering element are sequentially removable such that as each portion of the triggering element is removed, the elastic spacer sequentially moves from the second length toward the first length. The sequential movement of the elastic spacer from the second length toward the first length responsively urges the first and second substrates longitudinally toward one another to apply a predetermined amount of longitudinal force to the patient target site.