An apparatus, for use with a cochlear implant having a magnet and implanted within a patient having first and second ears, includes a first splint and a strap system, including at least a forehead strap and a chin strap, configured to position the first splint behind the first ear.

An apparatus, for use with a cochlear implant having a magnet and implanted within a patient having first and second ears, includes a first splint and a strap system, including at least a forehead strap and a chin strap, configured to position the first splint behind the first ear.

Arrangements described herein relate to systems, apparatuses, and methods for a disposable kit containing medical items configured for a medical device including a head cradle to support a head of a subject, the disposable kit includes a container that encloses a head cradle pad configured to be affixed to the head cradle, at least one fiducial marker configured to be disposed on a location at the head of the subject, and at least one enclosure configured to cover a portion of the medical device.

A rotary aspirator according to the present invention includes: a body portion which has a length in a front and rear direction, and has an outer circumferential surface formed as any one of a circular shape, an elliptical shape, and a polygonal shape in a lateral direction; a handle which is connected to a rear end of the body portion and has a smaller diameter than the rear end of the body portion so that a user moves the handle forward and rearward and rotates the handle in a state in which the user holds the handle by hand; and an absorbing member which is continuously and spirally wound in the front and rear direction of the body portion and absorbs nasal mucus of a target person.

A dry eye treatment device and method including a pliable thermal pack engageable upon a first side of a vibration ring is provided. The vibration ring has a second side adapted for positioning on the face of a user to communicate vibration to the eyelids of a user from the vibration ring, and heat or cold from a bulging portion of the thermal pack communicating through a pair of openings in the vibration ring. A cover forming a cavity on the face of the user to house the vibration ring and the thermal pack may also be employed.

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.

The invention relates to a flat wound care article having an essentially polygonal or ellipsoid base surface and at least one recess arranged on one side.

The present invention provides an improved bilateral compression device for post-operative surgical site, the bilateral compression device including a central cavity presented by an outerwall and a circumscribing sidewall, the central cavity in receipt of a post-operative pillow further comprising an outer membrane separated from an inner membrane for exerting a central compressive force towards the post-operative surgical area which varies from a surrounding compression force.

The present disclosure relates to fluid absorbers, along with a process for making the fluid absorber, which may be used, for example, by Parkinson's disease patients. The fluid absorber may include individual units that are folded into each other. The fluid absorber may be folded into a rectangle or square. The fluid absorber is then placed into an antimicrobial solution, and left to dry. In this way, a fluid absorber may have antimicrobial properties that reduce or eliminate tooth decay associated with hypersalivation. The fluid absorber is then placed inside the patient's mouth where it absorbs saliva until it becomes saturated. The fluid absorber may then be disposed.