The present invention relates in a first aspect to an adhesion material for use in an individual containing encapsulated phase-change material. In particular, the adhesion material is for cosmetical or medicinal use in the body of an individual. The adhesion material contains encapsulated phase-change material having preferably a phase transition temperature above 40° C., like above 55° C. The adhesion material is particularly useful for adhering elements, like dental restorations, e.g. crowns or bridge, or brackets on elements in the body of an individual, like teeth or implants. That is, the adhesion material is particularly useful for adhering material in dental applications. In another aspect, a method is provided allowing removing a bracket, a crown or bridge, from implants, abutments or teeth. Furthermore, dental implant restoration systems and kits for permanent fixation of implants allowing improved removal thereof are provided.

The present invention relates to an automatic oral sensor sterilizing and packaging system and, particularly, to an automatic oral sensor sterilizing and packaging system capable of automatically sterilizing an oral sensor and further packaging the oral sensor with disposable wrapping paper, comprising: a housing including a sterilization unit providing a sterilization region for sterilization of the oral sensor and/or a packaging unit providing a packaging region for packaging the oral sensor; and a transfer unit for making the oral sensor pass through at least one of the sterilization region and the packaging region.

A system and method for monitoring a medical procedure performed in a clinical environment is provided. An audio recorder is configured to produce a verbal data signal that is representative of a verbal communication occurring in the clinical environment, and a data analyzer is configured to detect an adverse condition based upon the verbal data signal. An alert module is configured to alert an operator upon the detection of an adverse condition.

A system and method for monitoring a medical procedure performed in a clinical environment is provided. An audio recorder is configured to produce a verbal data signal that is representative of a verbal communication occurring in the clinical environment, and a data analyzer is configured to detect an adverse condition based upon the verbal data signal. An alert module is configured to alert an operator upon the detection of an adverse condition.

A safety device for tethering an object during intraoral use, such as a dental finger driver. A tether includes a semi-rigid tip portion connected to a flexible, inelastic tail. The tip portion is oriented parallel with the length of the tail during use. The tail may be formed from a filament, such as nylon monofilament. The tip portion may be formed from plastic. The tip can be easily inserted through an aperture in the device being tethered, with the tail portion being pulled through the aperture and secured to the intraoral object. The tail portion may be secured by a knot, a stopper, or a loop formed in a second end of the tail, through which the tip may be passed.

A safety device for tethering an object during intraoral use, such as a dental finger driver. A tether includes a semi-rigid tip portion connected to a flexible, inelastic tail. The tip portion is oriented parallel with the length of the tail during use. The tail may be formed from a filament, such as nylon monofilament. The tip portion may be formed from plastic. The tip can be easily inserted through an aperture in the device being tethered, with the tail portion being pulled through the aperture and secured to the intraoral object. The tail portion may be secured by a knot, a stopper, or a loop formed in a second end of the tail, through which the tip may be passed.

A method of cleaning and lubricating a detached device within a sealed heat sterilizable container during the process of heat sterilization by using a liquid admixture comprised of a water-alcohol-glycerin-chlorhexidine solution.

Described herein are compositions in nanofiber form including one or more bioactive compounds releasably incorporated thereon. In one embodiment a composition is described comprising at least one nanofiber and at least one bioactive compound. The nanofibers are formed from a base material that is solubilized with the bioactive or bioactives in an aqueous based solvent solution and the base material and bioactives are together spun via electrospinning to form dry fibers with the bioactives chemically bonded to the nanofibers and the bioactives remaining stable during storage of the composition under ambient conditions substantially free of moisture. On exposure to moisture, the nanofibers dissolve, thereby releasing the bioactives.

Described herein are compositions in nanofiber form including one or more bioactive compounds releasably incorporated thereon. In one embodiment a composition is described comprising at least one nanofiber and at least one bioactive compound. The nanofibers are formed from a base material that is solubilized with the bioactive or bioactives in an aqueous based solvent solution and the base material and bioactives are together spun via electrospinning to form dry fibers with the bioactives chemically bonded to the nanofibers and the bioactives remaining stable during storage of the composition under ambient conditions substantially free of moisture. On exposure to moisture, the nanofibers dissolve, thereby releasing the bioactives.

A teeth surface stain removing apparatus removes stains on a teeth surface, and includes a sheet member capable of being attached to the teeth surface via an adsorptive member for adsorbing the stains, a teeth surface electrode disposed at a part of the sheet member, the part being attached to the teeth surface, and a charge supplier supplying negative charges to the teeth surface electrode in a state where the sheet member is attached to the teeth surface.