Karl Leibinger Medizintechnik Gmbh & Co Kg

Karl Leibinger Medizintechnik Gmbh & Co.

Karl Leibinger Asset Management Gmbh & Co. Kg.

Karl Leibinger Medizintechikgmbh & Co. Kg

Frank Reinauer

Jörg Mayer

Tobias Wolfram

Adem Aksu

Siegmund Luger

Marijan Vucak

Lorenz Gabele

Gwenn Swennen

Nils-Claudius Gellrich

Axel Waizenegger

Heiner Wild

Björn Rahlf

Harald Essig

Oliver Scheunemann

Majeed Rana

Daniel Milkau

Gwen Swennen

Ernst-Johannes Haberl

Veit Irion

Anita Grigore

Stefanie Grom

Ralf Leibinger

Martin Rücker

Wolfgang Müller

The invention relates to a maxilla repositioning implant () for three-dimensional precise alignment of a maxilla displacing portion () relative to a remaining maxilla portion () that is fixed to the skull, wherein the maxilla repositioning implant () comprises a base (), which has at least one plate () in which screw holes () are provided, wherein a portion of the material of the plate () defines, as a rim (), a respective screw hole () that is provided for receiving a bone screw () in order to ensure fastening, via the bone screw () to be inserted into the respective screw hole (), to the remaining maxilla portion () that is fixed to the skull, wherein the maxilla repositioning implant () also comprises a connection portion (), which is spaced apart from the base () by connecting bridges (), wherein the connection portion () comprises at least one plate () in which screw holes () are provided, and wherein a portion of the material of this plate () defines, as a rim (), a respective screw hole () in order to ensure fastening, via a bone screw () to be inserted into the respective screw hole (), to the maxilla displacing portion (), wherein two plates () of the base () are connected to each other via a retaining bracket ().

Maxilla repositioning implant comprising a retaining bracket

The invention relates to an implant () comprising a support structure () which is prepared for anchoring, following the contours of the bone, in a jaw- and/or cranial bone (), wherein at least one integrally attached post () protrudes from the support structure (), said post being designed to have a finished denture anchored thereto and the post () having a base () that is formed out of the support structure () and is completed by a distal end region () with the interposition of a radially enlarged region (). The invention also relates to a soft tissue displacement system () comprising an implant (), a manufacturing process for a soft tissue displacement system () and a planning process for manufacturing an implant ().

Implant comprising a radially enlarged post on the support structure, soft tissue displacement system, manufacturing process and planning process for manufacturing an implant

The invention relates to a bone implant () for correcting an incorrect position of a bone, the bone implant () having a first portion () for attachment to a first bone portion () and a second portion () for attachment to a second bone portion (), the bone implant () being prepared so that, when fixed to the bone, it orients the first bone portion () and the second bone portion () with respect to one another and keeps said portions at a distance from one another, the bone implant () having such a geometry and being adapted so as to force a predetermined orientation of the second bone portion () relative to the first bone portion (). The invention also relates to a method for producing such a bone implant ().

Bioresorbable bone implant and production method

Implant comprising composite powder with microstructured particles, obtained by a process in which large particles are bonded to small particles, wherein Therefore, the subject matter of the invention further are implants obtained by selective laser sintering of a composition comprising a composite powder, especially as an implant for applications in the field of neuro, oral, maxillary, facial, ear, nose and throat surgery as well as of hand, foot, thorax, costal and shoulder surgery.

Implant comprising a calcium salt-containing composite powder having microstructured particles

The invention relates to a bone positioning device () for use in the repositioning of bone sections relative to each other in case of dysgnathia, comprising a main body (), which has a bottom side (), which faces the lower jaw () and in which there are recesses () for receiving navigating aids () fixed to the lower jaw, and an opposite top side (), which faces the upper jaw and in which there are likewise recesses () for receiving navigating aids () fixed to the upper jaw, wherein at least one cutting-tool guide device () is attached to the main body ().

Bone positioning device for dysgnathia having a cutting-tool guide

The invention relates to a method for producing an implant which contains a composite powder comprising microstructured particles, obtainable by a method in which large polymer particles are bonded to small spherical calcium carbonate particles. Said calcium carbonate particles can be obtained by a method with the following steps: a) providing a calcium hydroxide suspension, b) introducing carbon dioxide or a carbon dioxide-containing gas mixture into the suspension from step a), and c) separating the calcium carbonate particles formed, while adding 0.3 wt.-% to 0.7 wt.-% of at least one amino trialkylene phosphonic acid.

Method for producing an implant using a calcium carbonate-containing composite powder comprising microstructured particles

The present application relates to an implantation set including a tool or an aid, and at least one bone contact member adapted thereto, therefore a device designed for direct contact with a bone, the bone contact member having a greater hardness in a region intended for contact by the tool or aid than the tool or aid in a region intended for contact with the bone contact member.

Implantation aid for the use of surface-sensitive implants

A cranial bone fastening device for temporarily fastening multiple cranial bone portions to a main body of a positioning device in order to orient the cranial bone portions relative to one another, wherein a pin-like fixing element portion is provided, one side of which is designed to contact the multiple cranial bone portions in order to secure the cranial bone portions to the main body of the positioning device upon interaction with a counter portion on the other side of the cranial bone portions.

Cranial bone fastening device for fastening a cranial bone portion to a positioning device

The invention relates to a bone implant for attaching to on a surface of a bone, including a base body whose lower side and/or upper side correspond(s) substantially to a deformation-free bone outer contour, wherein the outer dimensions of the base body are chosen such that the base body covers a specifically introduced deformation region for obtaining autologous bone material completely, wherein in the base body at least one slot is provided which is dimensioned such that it guides a bone marking and/or bone processing tool inserted in the slot in use.

Bone implant for the reconstruction of an osseous defect and for guiding a marking and/or processing tool for transferring required osteotomy situations

The invention relates to a method for producing an implant by means of a composite powder having micro structured particles having inhibiting calcium carbonate, wherein the composite powder is obtained by a method in that large polymer particles are joined to small calcium carbonate particles, wherein the calcium carbonate particles are obtained by a method in that calcium carbonate particles are coated with a composition which, in each case based on the total weight thereof, comprises a mixture of at least 0.1 wt % of at least one calcium complexing agent and/or at least one conjugated base which is an alkaline metal or calcium salt of a weak acid, together with at least 0.1 wt % of at least one weak acid.

Method for producing an implant comprising calcium carbonate-containing composite powder having microstructured particles having inhibiting calcium carbonate

The present invention relates to a (poly)hybrid implant made of one or more composite materials, having a polymer matrix and a ceramic-inorganic and/or inorganic component, wherein the polymer matrix has at least one component, selected from the group PDLLA; PLGA, PCL, HDPE, PE, UHMWPE, PEAK, PEEK, PP, PUR, and the ceramic-inorganic component has at least one calcium-phosphate-based component, preferably selected from the group HAP, &#x3b1;-TCP, &#x3b2;-TCP and CaCO. In addition, metallic components can also be introduced, preferably, but not exclusively containing elements such as Mg, Fe, Zn or Sr.

Hybrid implant made of a composite material

The invention relates to an implant for attaching to a bone, having bone support surfaces or bone formfitting sections which are inclined relative to each other in order to rest on the surface of the bone. Two bone formfitting sections are aligned relative to each other in a sub-region of the implant such that surrounding the bone in the sub-region secures the position of the implant. The invention also relates to a method for producing an implant according to the invention.

Implant for reinforcing a bone, comprising a bore vector specifying hole and surrounding plate for a jaw replacement, and implant production method

The present application relates to an eye socket covering grid that includes a curved main body with an external closing edge, a lower side which, in the implanted state, is facing the bone or bones forming the eye socket, and an upper side distant from the lower side, wherein at least one optically identifiable linear channel for representing at least one insertion vector is formed on the upper side. The application also relates to a method for producing such an eye socket covering grid, in particular an eye socket covering grid adapted in a patient-specific manner.

Method for manufacturing a patient-specific eye socket covering grid and patient-specific eye socket covering grid

The invention relates to a medical synthesis system as well as to a method of connecting a multipart medical synthesis system. The medical synthesis system in this respect includes at least one supporting element and at least one synthesis element, wherein the supporting element is provided for fastening in an organic structure. In this respect, the synthesis element is provided for the fastening to the already fastened supporting element. The synthesis element and the supporting element form a non-releasable coherent unit during application.

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Emmingen-Liptingen, Germany

Frank Reinauer