Disclosed are nasal dressings and nasal stents comprising a collagen foam. Also disclosed are methods of making and using such nasal dressings and nasal stents. In an embodiment, a nasal dressing or nasal stent is formed by a method comprising the steps of: forming an aqueous mixture of from 5 to 25 wt % of acid-soluble collagen and from 75 to 95 wt % of collagen fibers, both based on the total solids content of the aqueous mixture, placing the aqueous mixture into a mold, freeze-drying the aqueous mixture while in the mold, thereby forming a collagen foam, and cross-linking the collagen foam.

A health band for a human body may include a band part having a through hole formed at a predetermined position such that a large amount of air for breathing by the respiratory system of the human body is introduced; and a protruding member which is formed so as to surround the through hole while blocking the through hole so as to prevent substances harmful to the human body contained in the air introduced through the through hole from flowing into the respiratory system.

Embodiments relate generally to systems and methods for shaping an external nasal cast. A nasal cast bender may comprise a base; and a protrusion protruding upwards from the base portion, wherein the protrusion comprises a handle and a bending surface comprising a convex profile; wherein the bending surface is configured to shape an external nasal cast.

Various devices and methods useful for providing vasocompression to a patient who is undergoing chemotherapy treatment.

Provided is a facial patch including a support, a pressure-sensitive adhesive layer, and a release layer in this order, in which (a) the pressure-sensitive adhesive layer satisfies the following conditions (a-1) to (a-3): (a-1) the pressure-sensitive adhesive layer contains a styrene-isoprene-styrene block copolymer, a tackifier resin, and a softening agent; (a-2) the ratio (mass ratio) of the styrene-isoprene-styrene block copolymer and the tackifier resin is 1:2 to 1:4; and (a-3) the content of the softening agent is 40% to 60% by mass; and (b) the support has elastic moduli with a Young's modulus of 0.01 GPa to 0.5 GPa, and also provided is a method for producing the facial patch, the method including a step of forming a pressure-sensitive adhesive layer on the upper surface of the release layer.

Provided is a facial patch including a support, a pressure-sensitive adhesive layer, and a release layer in this order, in which (a) the pressure-sensitive adhesive layer satisfies the following conditions (a-1) to (a-3): (a-1) the pressure-sensitive adhesive layer contains a styrene-isoprene-styrene block copolymer, a tackifier resin, and a softening agent; (a-2) the ratio (mass ratio) of the styrene-isoprene-styrene block copolymer and the tackifier resin is 1:2 to 1:4; and (a-3) the content of the softening agent is 40% to 60% by mass; and (b) the support has elastic moduli with a Young's modulus of 0.01 GPa to 0.5 GPa, and also provided is a method for producing the facial patch, the method including a step of forming a pressure-sensitive adhesive layer on the upper surface of the release layer.

A compression garment system and method that may include a head garment portion configured to be donned on a head of a body. The compression garment and method may further include a neck garment portion configured to be donned on a neck of the body. A controller may be configured to control pressure applied by each of one or more head pressure applying regions and/or each of one or more neck pressure applying regions to move lymph at least from the head towards the neck.

A compression garment system and method that may include a head garment portion configured to be donned on a head of a body. The compression garment and method may further include a neck garment portion configured to be donned on a neck of the body. A controller may be configured to control pressure applied by each of one or more head pressure applying regions and/or each of one or more neck pressure applying regions to move lymph at least from the head towards the neck.

A nose compression device to treat a nosebleed. The device has a wire frame with a straight middle section and two side sections angled with respect to the middle section to apply an inward compression against an outside of the person's nose. The device also includes a support member attached to the wire frame. And, a single nasal sponge attached to the body and having a central sponge portion and two opposing sponge end portions, each of said two opposing sponge end portions configured for insertion into the person's nasal passages.

An absorbent insert of compressed matrix of absorbent material, including a filler dispersed therein to improve stiffness/rigidity of the insert and controls the absorbency of the compressed absorbent material. The insert is pre-shaped and sized for inserting into a tooth cavity, such as a pulp chamber or a root canal space. The compressed insert expands or swells upon absorbing fluid within the tooth cavity, so as to more completely dry the tooth cavity. The absorbent insert also serves as a substrate of an applicator for medical agent to be applied to a tooth cavity. The absorbent insert is provided (e.g., coated or impregnated) with a medical agent, which medical agent is released into the tooth cavity as the absorbent material absorbs fluid in the tooth cavity.