The present disclosure relates to a two-component medical device for closing a wound or incision. The two-component device comprising a first and second component, each comprising an adhesive-backed anchoring member having one edge referred to as the wound edge. The adhesive-backed anchoring members are produced from a polymeric film sheet. Disclosed are instances wherein the adhesive-backed anchoring members are characterized by the presence of one or more discontinuities in the polymeric film sheet.

The present disclosure relates to a dressing (100) comprising a backing layer (101), an adhesive skin contact layer (102) and a first release liner (103), wherein the adhesive skin contact layer (102) comprises a central portion (102a) and an edge portion (102b) surrounding the central portion (102a). The first release liner (103) is configured to be releasably attached to at least the central portion (102a) of the adhesive skin contact layer (102). The dressing (100) comprises a second release liner (104) arranged between the first release liner (103) and at least part of the edge portion (102b) of the adhesive skin contact layer (102).

The methods, procedures, kits, and devices described herein assist with the healing process of tissue that was previously or simultaneously treated for a therapeutic or cosmetic effect. The methods, procedures, kits, and devices described herein can also provide temporary simulated results of a cosmetic procedure to allow for visual assessment to select the type of procedure or for treatment planning in advance of the surgical procedure.

A hemostatic surface application device having a region of hemostatic foam for contact with a patient's skin where a wound exists or is created, the device includes: a release layer, the release layer in contact with a hemostatic flexible foam section, and a structural foam layer having a front side and a back side surrounding the hemostatic flexible foam layer, forming a generally central hemostatic surface exposed through the front side of the surrounding structural foam layer, and a support layer adhered to the backside of the structural foam layer.

The invention relates to a therapeutic adhesive tape for use in medical or sporting applications. The therapeutic tape is configured to be applied to the skin of a user. The tape comprising: a base layer having a face side and a back side, the base layer being composed of a combination of recycled polyethylene terephthalate (hereinafter: RPET) and an elastic material, and an adhesive layer deposited on one of said face side or back side of the base layer for attaching the tape to the skin of the user.

A convenient sports tape, comprising a package body and a tape body; the package body has at least one transparent top sheet, a bottom sheet matching the top sheet with its edge connected to that of the top sheet, and a housing space formed between the top sheet and the bottom sheet, the housing space can store and clamp the tape body; the tape body is provided with at least one adhesion section, and a positioning section configured on one end of the adhesion section; the tape body has three layers in total, made up of a tape layer, an adhesive layer, and a releasing layer of the same shape; the tape layer can be configured according to the marbling of lean flesh.

The disclosed securement tape strip comprises a tape having a midsection, a stabilizing section, and a wrapping strip. The tape strip has an adhesive along the midsection to adhere the tape strip to a substrate. The wrapping strip can include an adhesive for wrapping the wrapping strip around a device to hold the device securely in place on the substrate. The tape strip can include a perforation set along the midsection. The perforation set can be useful in removal of the tape.

A nasal dilator, comprising a plurality of laminated components, wherein each of the laminated components comprises a first major surface that faces in a first direction and a second major surface that faces in a second direction, the plurality of laminated components comprises at least one resilient member, each of the at least one resilient member comprises a first end at a first edge of the nasal dilator and a second end at a second edge of the nasal dilator, each of the at least one resilient member extends from the first end to the second end in a direction parallel to a longitudinal axis of the nasal dilator, the plurality of laminated components comprises a first component and a second component, an entirety of the second major surface of the first component is of a first color, an entirety of the second major surface of the second component is of a second color, and at least a portion of the second major surface of the first component and at least a portion of the second major surface of the second component is a visibly exposed surface of the nasal dilator.

The present invention pertains to an integrated wound dressing device for treatment of an insertion site of percutaneous and drug delivery devices. The integrated wound dressing device preferably comprises a transparent film layer having a bottom side, a top side and a perimeter. The bottom side is coated with an adhesive impregnated with an antimicrobial agent. The transparent film has a radius cutout between a central opening and the perimeter. A liquid crystal temperature sensitive film with an adhesive placed on the top side of the transparent film layer is preferably near and around the central opening. The dressing also has a layer of double folded release paper below the bottom side of the transparent film layer. The preferred TLCs used are cholesteryl esters with a preferable temperature detection range of 35-40° C. The preferred antimicrobial agent is chlorohexidine gluconate (CHG).

An adhesive article that remains securely bonded to a substrate until a stimuli is applied. The article may be embodied as an adhesive tape, a bandage, or as other articles. The stimuli may be a change in temperature or application of a reduction that causes a structure within the article to break, creak, or otherwise disrupt to expose the adhesive to a solvent, such as via a difference in Coefficient of Thermal Expansion (CTE) or by exposing the article to a glass transition temperature.