Biomet Manufacturing Corporation

Biomet, Inc.

St. Jude Medical Puerto Rico LLC

Other

Covidien LP

Zimmer Gmbh

Bridgestone Bandag, LLC

Medtech S.a.

Synthes Usa, LLC

Boise Cascade Company

Blomet Manufacturing, LLC

Glaxosmithkline LLC

John Robert White

Jason D Meridew

Robert G Metzger

Mark A Bollinger

Seth Anderson Nash

David R Brown

Tyler D Witt

Brian M May

Keith R Berend

William Jason Slone

W Jason Slone

Mark Scrafton

Troy W Hershberger

Aaron P Smith

Kirk J Bailey

Andrew T Forsberg

Daniel L Martin

Lance Dean Perry

Louis-Philippe Amiot

Jon C Serbousek

Jody L Claypool

Russell David Terwey

Gregory J Denham

Jacy C Hoeppner

Ryan John Schoenefeld

Jennifer E Woodell-May

Alan Peter Lewis

Jonathan Henry Ellis

Brian David Salyer

Robert Tadlock

Joseph Mcginty

Charles Burris

Steven Faes

Wade Patterson

William R Fiehler

Bryan Morrison

Wanda Dent

Annelise Galloway

Charles Senness

Russell M Parrott

Roy C Wiley

Mukesh Kumar

Volker Germaschewski

Adolph V Lombardi

Michael E Berend

John S Lindsay

Zdenka Ludmila Jonak

Jeff D Lewis

Kurt N Schmidt

Frederik Gelaude

Elizabeth A Schlueter

Stephanie Jane Clegg

William J Hamman

Tim Clijmans

Andreas Carl Pfahnl

Tony Siebeneck

Kortney Wawrzyniak

Eric Dobrzynski

Jeffrey C King

Steven W Prunchak

Keith R Gerhart

J Scott Owens

David Ruth

Alexis Paul Godillot

Richard J O'Donnell

J Scott Deming

Thomas C Raish

Trent Bauters

Paige McKinley

Neill O'Quinn

Steven William Prunchak

Lance D Perry

Michael Canada

Rory Kiphart

A system and method for using augmented reality device for use during a surgical procedure are described. A system may include an augmented reality device to present a virtual indication, such as a virtual indication of a surgical instrument, a force vector, a direction, or the like. The augmented reality device may present a virtual aspect of a procedure, such as a virtual animation of a step of a procedure. The augmented reality device may present a virtual object, indication, aspect, etc., within a surgical field while permitting the surgical field or aspects of the surgical field to be viewed through the augmented reality display (e.g., presenting virtual objects mixed with real objects).

Augmented reality surgical technique guidance

A method of implanting a hip joint prosthesis into a patient can include obtaining image data of hip joint anatomy of the patient. Physical activities that the patient desires to participate in subsequent to implanting the hip prosthesis can be determined. A size and an initial placement of the hip joint prosthesis based on the image data can be determined. A desired range of motion of the hip joint prosthesis based on the determined physical activities can be determined. A plan can be created comprising a desired implanted location of the hip joint prosthesis and based on the desired range of motion. The plan can be incorporated onto a guide. The plan can be executed with the guide thereby implanting the hip joint prosthesis into the patient at the desired implanted position.

Method for implanting a hip prosthesis and related system

A tread extraction assembly is provided. The tread extraction assembly includes a base frame, a first clamping assembly, and a second clamping assembly. The base frame defines a leading edge. The first clamping assembly includes a first clamp movable relative to the base frame. The second clamping assembly is coupled to the base frame and includes a second clamp positioned proximate to the leading edge. The tread extraction assembly also includes a linear rail and a linear bearing. The first clamping assembly is coupled to the linear bearing and movable along the linear rail by a linear actuator.

Molded article extractor and method

Systems and methods are described herein for resurfacing bones, and in particular, for detecting and resurfacing one or more femoroacetabular impingements (FAIs). A FAI resurfacing controller may be used to perform this detecting and resurfacing of FAIs. The FAI resurfacing controller may include a bone model generator to receive bone imaging and to generate a model of at least one osteophyte and of a surface of a native bone surrounding the at least one osteophyte. The FAI resurfacing controller may include an osteophyte identifier to set a virtual 3D boundary surface between native bone surface and the at least one osteophyte. The FAI resurfacing controller may include a resurfacing navigator to generate and output a navigation file. The navigation file may include the model with the 3D boundary surface between native bone surface and the at least one osteophyte.

Robotized system for femoroacetabular impingement resurfacing

A method of manufacturing includes cutting a first natural or non-composite veneer sheet to a first length, cutting a second natural or non-composite veneer sheet to the first length, coating an inner surface of the first natural or non-composite veneer sheet with an adhering means, coating an inner surface of the second natural or non-composite veneer sheet with an adhering means, coating a plurality of veneer strands with an adhering means, placing the plurality of veneer strands on the inner surface of the first natural or non-composite veneer sheet, placing the second natural or non-composite veneer sheet on top of the plurality of veneer strands to create a mat, compressing the mat in an unheated pre-press, and compressing the mat in a hot press at an elevated temperature to create a panel.

Method for manufacturing wood products formed from natural veneer sheets and veneer strands

A stent delivery system includes a handle and an elongate catheter extending from the handle. The elongate catheter includes an inner member, an outer member mounted about the inner member and adapted for longitudinal movement relative to the inner member from an extended position to a retracted position and a stent mounted about the inner member. The stent delivery system also includes a thumbwheel mounted to the handle. The thumbwheel is adapted for rotational movement to cause corresponding movement of the outer member from the extended position to the retracted position. In some examples, the stent delivery system may include a lock member adapted to engage at least one of the outer member and the thumbwheel to prevent movement thereof when the lock member is secured relative to the handle.

Stent delivery system

A method of preparing a surgical plan comprises video capturing a range of motion of an anatomic joint of a patient to obtain a range of motion video, registering the range of motion video to two-dimensional images of a skeleton of the patient, identifying potential impingement and stability issues in the anatomic joint based on the range of motion video, templating a prosthetic implant on two-dimensional images of the anatomic joint using the identified potential impingement and stability issues of the anatomic joint to obtain position and orientation data, and electronically saving the position and orientation data of the prosthetic implant for use with a surgical navigation system. A system for planning and performing a surgical procedure comprises a motion capture system, an x-ray system, an electronic modeling system, and a surgical navigation system.

Method and system for planning and performing arthroplasty procedures using motion-capture data

Systems and methods for using an augmented reality device during patient diagnosis. A method may include capturing an image of a patient, and presenting using an augmented reality display, while permitting the patient to be viewed through the augmented reality display, a virtual feature corresponding to anatomy of the patient obtained from the image. The method may include detecting impingement of the anatomy of the patient based on the image and displaying on the augmented reality display, an indication of the impingement at the virtual feature, such as by changing an attribute of the virtual feature.

Augmented reality diagnosis guidance

A loader device includes a support pedestal movable over a range of longitudinal travel along a longitudinal axis, a support carriage movably mounted to the support pedestal, a loader actuator, and a dismount actuator. The support carriage is movable over a range of vertical travel along a normal axis, which is perpendicular to the longitudinal axis. The support carriage has a support arm adapted to support a tire casing. The loader actuator and dismount actuator are respectively adapted to selectively move: (1) at least a portion of a tire casing supported upon the support carriage in a loading direction along the longitudinal axis off of the support arm onto the expandable rim hub and (2) at least a portion of a tire casing supported upon the expandable rim hub in an opposing unloading direction off of the expandable rim hub and onto the support arm of the loader device.

Automatic system and method for mounting and dismounting tire casing on expandable rim hub in retreading operations

A stent delivery system includes a handle and an elongate catheter extending from the handle, and defining a leading end and a trailing end, and having a longitudinal axis. The elongate catheter includes an inner member, an outer member mounted about the inner member and adapted for longitudinal movement relative to the inner member from an extended position to a retracted position and a stent mounted about the inner member. The stent delivery system also includes a thumbwheel mounted to the handle and operatively connected to the outer member, and a lock member releasably mountable to the handle. The thumbwheel is adapted for rotational movement to cause corresponding movement of the outer member from the extended position to the retracted position. The lock member is adapted to engage at least one of the outer member and the thumbwheel to prevent movement thereof when the lock member is secured relative to the handle, and is adapted to release the at least one of the outer member and the thumbwheel when the lock member is released relative to the handle. The lock member may be adapted to engage each of the outer member and the thumbwheel to prevent respective movement thereof when the lock member is secured relative to the handle and adapted to release each of the outer member and the thumbwheel when the lock member is released relative to the handle.

An orthopedic implant includes a first portion including at least one feature modified to be patient-specific and match the anatomy of a specific patient from a three-dimensional digital image of a patient's joint using computer modeling. The orthopedic implant includes a non-custom inner bone-engaging surface including a plurality of planar surfaces configured for engagement with non-custom bone cuts.

Patient-modified implant

Growing community of inventors

Winona Lake, IN, United States of America

John Robert White