A mouth-insertable device, including a main body having a cylindrical shape, a first end disposed at an end of the main body, and a second end disposed at another end of the main body opposite from the first end, wherein the main body has a size to fit between an inner upper lip and an upper gum line of a user.

A method for treating sleep-disordered breathing in a patient includes prior to sleeping, placing a sleep strip on a face of the patient, the sleep strip being configured to maintain lips and/or a jaw of the patient in a closed posture, and the sleep strip including a first layer comprising an adhesive configured to attach the sleep strip to the face of a patient, the first layer having an opening extending therethrough, the opening being located above the lips of the patient, and a mesh layer covering at least the opening of the first layer, the mesh layer being configured to allow air to flow therethrough; and disposing a device configured to facilitate stable breathing patterns on a face or in a mouth of the patient.

An emergency trauma stretch bandage cap shaped as a skull cap with roll able edges capable of holding hot or cold packs, which is placed on the cranium to cover the crown, forehead, back of the head, ears, sides of the head around the ears, and the temples of an injured patient with minimal movement of the neck and spine made of two or more layers of a stretchable warp knit fabric cut and sewn to form a form-fitting head bandage shape to apply sufficient pressure to suppress bleeding.

An emergency trauma stretch bandage cap shaped as a skull cap with roll able edges capable of holding hot or cold packs, which is placed on the cranium to cover the crown, forehead, back of the head, ears, sides of the head around the ears, and the temples of an injured patient with minimal movement of the neck and spine made of two or more layers of a stretchable warp knit fabric cut and sewn to form a form-fitting head bandage shape to apply sufficient pressure to suppress bleeding.

A therapeutic device has a bridge portion adapted for releasable adherence to a patch of skin so as to lift the patch of skin above a sensitive underlying treatment site in reducing discomfort or pain associated with tissue compression at the treatment site. The bridge portion is elevated above the treatment site with an exposed adhesive facing the patch of skin to be lifted and/or stretched outwardly. With the application of pressure to elastically deform the device from its original neutral configuration, the bridge portion is brought into contact with the patch of skin, adhering the skin to the adhesive. When the pressure is removed, the device rebounds and generally reassumes its original configuration with the bridge portion lifting the attached patch of skin.

A system comprising a handpiece and drive system configured to removably couple to a proximal end of a housing. A scalpet assembly is configured to removeably couple to the housing, and includes a scalpet array comprising at least one scalpet configured for rotation. The scalpet array is configured to harvest dermal plugs via fractional resection. A collection chamber is configured to collect the dermal plugs, and to house formation of an injectable filler by mincing the dermal plugs, and mixing the dermal plugs with a carrier. The injectable filler is configured for bulk fill. The collection chamber includes a loading port, and a cannular syringe is configured to mate with the loading port to receive the injectable filler, and to deliver the injectable filler for the bulk fill.

A system comprising a handpiece and drive system configured to removably couple to a proximal end of a housing. A scalpet assembly is configured to removeably couple to the housing, and includes a scalpet array comprising at least one scalpet configured for rotation. The scalpet array is configured to harvest dermal plugs via fractional resection. A collection chamber is configured to collect the dermal plugs, and to house formation of an injectable filler by mincing the dermal plugs, and mixing the dermal plugs with a carrier. The injectable filler is configured for bulk fill. The collection chamber includes a loading port, and a cannular syringe is configured to mate with the loading port to receive the injectable filler, and to deliver the injectable filler for the bulk fill.

An oxygen scavenging dressing includes a patient interface layer, an absorbent layer, a foam layer, an oxygen scavenging layer, and a film layer. The film layer is configured to seal with a patient's skin and define an inner volume within which the patient interface layer, the absorbent layer, the foam layer, and the oxygen scavenging layer are positioned.

Compression garments may include mitts and tightening apparatus to don, or put on, such compression garments. The mitts may be configured to receive a user's hand such that the user can move one or more portions of the garments using the mitts. The tightening apparatus may allow a user to selectively tighten or loosen the garments about the user's body portions. Once donned, the compression garments may apply pressure to one or more regions of the user's body such as, e.g., arm regions, shoulder regions, torso regions, and neck regions.

Compression garments may include mitts and tightening apparatus to don, or put on, such compression garments. The mitts may be configured to receive a user's hand such that the user can move one or more portions of the garments using the mitts. The tightening apparatus may allow a user to selectively tighten or loosen the garments about the user's body portions. Once donned, the compression garments may apply pressure to one or more regions of the user's body such as, e.g., arm regions, shoulder regions, torso regions, and neck regions.