Woodwelding Ag

Spinewelding Ag

Ww Technology Ag

Stryker European Holdings I LLC

Nobel Biocare Services, Ag

Stryker Trauma Gmbh

New Dent Ag

Woodwelding Sa

Urs Weber

Jörg Mayer

Philipp Seiler

Andrea Müller

Stephanie Mehl

Milica Berra

Marcel Aeschlimann

Mario Lehmann

Laurent Torriani

Andrea Mueller

Elmar Mock

Christopher Rast

Thomas Knecht

Hansen A Yuan

Klaus Dorawa

Andreas Wenger

Frank Martin Phillips

Stephen Hochschuler

Nils Zander

Stephanie Goebel-Mehl

Ulrich Berlemann

Robert Sonntag

Joerg Mayer

Jorg Weitzel

Thierry Ziegler

Roger Staudenmann

Peter Perler

Peter Schwenter

Jörg Weitzel

Ibrahim ÜNal

Marcel Siegfried

Milicia Berra

Andrea Muller

Eimar Mock

Seiler Philipp

Torriani Laurent

A system can be configured to record a position and orientation of a dental component. The system can include a coping and a replica. The coping can include an anti/rotational feature that is configured to mate with an anti-rotational feature of a dental component. The coping can also include an orientation feature that is configured to convey the orientation of the dental component. The replica can include a first anti-rotational feature that corresponds to the anti-rotational feature of the dental component. The replica can also include a second anti-rotational feature that does not correspond to the anti-rotational feature of the dental component.

Dental components and methods to align dental components

An implant or endoprosthesis suitable to be implanted in human or animal tissue includes two (or more than two) parts to be joined in situ. Each one of the parts includes a joining location, the two joining locations facing each other when the device parts are positioned for being joined together, wherein one of the joining locations includes a material which is liquefiable by mechanical vibration and the other one of the joining locations includes a material which is not liquefiable by mechanical vibration and a structure (e.g. undercut cavities or protrusions) suitable for forming a positive fit connection with the liquefiable material. The joining process is effected by pressing the two device parts against each other and by applying ultrasonic vibration to one of the device parts when the two parts are positioned relative to each other such that the two joining locations are in contact with each other.

Device to be implanted in human or animal tissue and method for implanting and assembling the device

A spine stabilization device having an interbody spacer shaped to be inserted between a vertebral body of an upper vertebra and a vertebral body of a lower vertebra. The device further includes a fixation device to be inserted after placement of the interbody spacer, the fixation device having a support portion securing the interbody spacer against escaping from between the vertebral bodies into a ventral direction. The support portion rests against a portion of an anterior surface of the interbody spacer, and includes an anchor. The anchor has an anchoring material portion that is inserted, in a liquid state, into cancellous bone tissue of at least one of the vertebral bodies of the upper and lower vertebra, to thereby infiltrate the cancellous bone tissue, and to harden thereafter so as to fix the support portion to the vertebral body.

Spine stabilization device, and method and kit for its implantation

A perforated sheath is anchored in a tissue opening with the aid of a tool, wherein the anchorage is achieved with the aid of mechanical vibration and a material which is liquefiable by the vibration. The tool includes a vibrating element and a counter element. Distal portions of both elements are introduced into the sheath to be in contact with each other at an interface. The vibrating element is connected to a vibration source and the vibrating element and the counter element are held against each other for effecting liquefaction of the liquefiable material at the interface. Under the effect of the force applied to the vibrating and counter element for holding them against each other, the liquefied material flows from the interface through the sheath perforation and penetrates the tissue.

Device and method for establishing an anchorage in tissue

The fusion device for fusing a synovial joint of a human or animal patient, in particular a human facet joint, finger joint or toe joint, includes two pin-shaped anchorage portions and arranged therebetween a stabilization portion. The anchorage portions include a thermoplastic material which is liquefiable by mechanical vibration. The stabilization portion preferably has a surface which is equipped for enhancing osseointegration. The anchorage portions have a greater thickness and a greater depth than the stabilization portion. Then the fusion device is pushed between the articular surfaces and mechanical vibration, in particular ultrasonic vibration, is applied to the proximal face of the fusion device. Thereby the liquefiable material is liquefied where in contact with the bone tissue and penetrates into the bone tissue, where after re-solidification it constitutes a positive fit connection between the fusion device and the bone tissue.

Method for fusing a human or animal joint as well as fusion device and tool set for carrying out the method

A medical method of affixing an element to a surface of dentine, tooth enamel, bone tissue, or corresponding substitute material. The method includes the steps of: providing an attachment composition, the attachment composition having a mixture of: a thermoplastic component; and a hardenable (for example curable) component. The hardenable component is different from the thermoplastic component. The method further includes the steps of: positioning the attachment composition relative to the surface of dentine, tooth enamel, bone tissue, or corresponding substitute material; and activating the attachment composition to attach to the surface or to attach to the element positioned relative to the surface. The step of activating the attachment composition includes activating the attachment composition by means of mechanical vibration.

Affixing an artificial element to a surface of dentine, enamel, bone, or a corresponding substitute material

A punching device for preparing a recess in a bone has a punching tool usable for such a punching device. An implant usable with the punching tool is provided and a method for preparing a recess in a bone are disclosed. The punching device comprises an ultrasonic sonotrode and a punching tool which is fixable to the sonotrode at its proximal extremity. At its distal extremity, the punching tool has a thin-walled portion having a non-rotational symmetric cross-section. By ultrasonic vibration of the punching tool, the thin-walled portion can be forced into a bone thereby preparing a recess of which is not rotationally symmetric. Subsequently, an implant can be held in such recess. Due to its lack of rotational symmetry, the implant may absorb rotational forces around its longitudinal axis.

Device and method for preparing a recess in a bone

A surgical method is provided, the method including the steps of: providing an artificial or allograft flexible planar structure; providing an implant, the implant including material liquefiable by mechanical oscillation, exposing a surface region of hard tissue or hard tissue substitute material; positioning the implant on an exposed area of the hard tissue or hard tissue substitute material; and fastening the implant to the hard tissue or hard tissue substitute material by impinging the proximal end of the implant with mechanical oscillation and simultaneously pressing the implant against the hard tissue or hard tissue substitute material while the distal end of the implant protrudes into a cavity of the hard tissue or hard tissue substitute material and regions of the liquefiable material are in contact with the hard tissue or hard tissue substitute material, and thereby liquefying at least a portion of the liquefiable material, and letting the liquefiable material resolidify.

Surgical method, kit of parts, and implant

A system and method of angularly stable fixation of an implant on a bone includes the steps of making at least one hole in the bone by means of a bone drill. An implant is placed on the bone in a desired position and joining the implant with the bone, such that the implant is prevented from rotation about its attachment point. A system is provided for use in the above described method. The system comprises a bone drill, an implant and a sonotrode for angularly stable fixation of the implant on the bone. The system can further comprise a joining element to join the implant with the bone.

Angularly stable fixation of an implant

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Evilard, Switzerland

Urs Weber