A tool assembly for mounting a dental abutment includes a first tool, the first tool having an axis of elongation, a first end configured to engage, in use, the abutment, and a second end, where a first portion of the first tool at or near the first end has a peripheral wall and, opposite the wall, a first opening extending along all or part of the first portion, a second opening open in an axial direction is disposed at the first end, the tool assembly further including a second tool configured to releasably engage a fixing element, where a contiguous space is defined between the first opening and the second opening whereby, in use, the fixing element, or the fixing element attached to the second tool, may pass through the first opening and the second opening to permit secure fixing of the abutment to an implant or frame using the second tool.

The invention relates to a treatment system (I) for cleaning a component contaminated by biofilm, more particularly for cleaning bacterially contaminated surfaces of bone implants or dental implants (30), the treatment system comprising at least two conductor elements (2, 4) connected to an electrical supply unit (10) to form an electrical circuit. One of the conductor elements can be brought into electrical contact with the component in need of treatment. The object of the invention is to provide a treatment system of this type which allows a particularly acceptable and flexible treatment. To this end, according to the invention at least one of the conductor elements (2, 4) is designed as a diamond electrode (26).

Methods, apparatuses, devices, and computer program products are disclosed for improved sanitization. An example device includes a sanitizing element that outputs a sanitizing agent. The device also includes a scanning device that generates scanning data of the physical form of the object. The device further includes a controller operatively coupled to the sanitizing element and the scanning device. The controller determines the output of the sanitizing agent during operation of the scanning device, receives the scanning data generated by the scanning device, and determines one or more areas of the object failing to receive sufficient contact with the sanitizing agent based upon the scanning data and sanitizing agent output.

Embodiments of the present invention provide an osseointegrative implant and related tools, components and fabrication techniques for surgical bone fixation and dental restoration purposes. In one embodiment an all-ceramic single-stage threaded or press-fit implant is provided having finely detailed surface features formed by ceramic injection molding and/or spark plasma sintering of a powder compact or green body comprising finely powdered zirconia. In another embodiment a two-stage threaded implant is provided having an exterior shell or body formed substantially entirely of ceramic and/or CNT-reinforced ceramic composite material. The implant may include one or more frictionally anisotropic bone-engaging surfaces. In another embodiment a densely sintered ceramic implant is provided wherein, prior to sintering, the porous debound green body is exposed to ions and/or particles of silver, gold, titanium, zirconia, YSZ, α-tricalcium phosphate, hydroxyapatite, carbon, carbon nanotubes, and/or other particles which remain lodged in the implant surface after sintering. Optionally, at least the supragingival portions of an all-ceramic implant are configured to have high translucence in the visible light range. Optionally, at least the bone-engaging portions of an all-ceramic implant are coated with a fused layer of titanium oxide.

The present disclosure provides a dental implant packaging container including: a see-through body unit in which upper and lower sides are open to form an accommodation space so that a dental implant fixture is accommodated therein and which is made of a material through which UV light for surface modification passes; a first cap unit which includes a hollow first cap body configured to cover an upper end portion of the accommodation space, a first fixing part protruding from a lower portion of the first cap body and having a coupling surface formed on an outer side portion, and a protruding part provided to protrude from the first fixing; a hollow holder unit which has an outer circumferential portion coupled to an inner circumference of the see-through body unit and an inner circumferential portion coupled to the coupling surface to mediate the connection between the see-through body unit and the first cap unit; and a second cap unit which includes a second fixing part fitted and coupled to a lower end portion of the see-through body unit and a base part provided on an inner side end of the second fixing part so that a lower end portion of the fixture is seated thereon.

A process for the preparation of a sterilized ceramic body including or essentially consisting of stabilized zirconia of a defined colour, including the steps of: providing a ceramic primary body including or essentially consisting of stabilized zirconia of a first colour A, and sterilizing the primary body using radiation sterilization whereby the primary body undergoes a colour change to a colour B. The process includes the further step of irradiating the sterilized primary body with electromagnetic radiation of at least one wavelength lying in the wavelength band ranging from 150 nm to 700 nm to induce an at least partial reversal of the colour change to obtain a colour C of the sterilized ceramic body, the colour C complying with the following requirements in the CIELAB colour space: L* being from 54 to 95, a* being from −15 to 15 and b* being from −15 to 15.

A dental implant with an implant extension which are formed along a longitudinal axis: the dental implant has an apical end, a coronal end and a section for receiving; securing an abutment; the implant extension is formed in one piece with the implant; extends away from an end face of the apical end along the longitudinal axis, the implant extension having a first section along the longitudinal axis with an annular constriction which is directly connected to the end face of the apical end of the implant; the implant breaks off from the implant extension at the constriction, along the longitudinal axis following the first section, wherein the second section, splined shaft section being further away from the implant than the first section, perpendicular to the longitudinal axis, an outer annular groove being designed to hold the implant extension by clamping the groove in the direction of the longitudinal axis.

The invention relates to a medical assembly, preferably a sterilized one, comprising a medical article (5) and a package containing said article, said package comprising a hollow support element (2) inside which said article (5) is free, a first protective element (3), called a stopper, which can be coupled to the support element (2) of said article, such that the support element (2) has a grip part (20) that protrudes from said stopper (3), and a second hollow protective element (4), called a cover. Said cover can be coupled to the stopper (3) in such a way as to delimit, in cooperation with said stopper (3), a chamber (8) inside which there extends said grip part (20) of the support element, and, in the state when the cover is coupled to the stopper, a part of the stopper (3) protrudes from the cover (4).

Dental implant embodiments comprising one or more non-annular cutaways from a portion of the crown are described. In some embodiments, cutaways, which are implantable beneath the bone line, are orientable during implantation by reference to a dental implant positioning tool to which the dental implant is mated in a known orientation. Mating, in some embodiments, is secured by a detent system which reversibly interlocks the positioning tool and the implant. In some embodiments, a surface of a cutaway is provided with protrusions which stimulate bone regrowth into the volume which the remainder of the cutaway provides.

A device for treating an artificial bone implant with blood, the device comprising: a container configured to accommodate an artificial bone implant and be filled with blood, wherein the container comprises an opening and a cover configured to cover the opening of the container. Additional embodiments of the device and methods for using the same are disclosed herein.