BLUEPRINT Patient Specific Instrumentation

FDA registration

Tornier S.A.S.·1 product·🇫🇷 France

BLUEPRINT Patient Specific Instrumentation

FDA registration

IMASCAP·1 product·🇫🇷 France

BLUEPRINT Patient Specific Instrumentation

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

FDA classification

FDA Class 2 ·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

INBONE

FDA registration

WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

Stryker

FDA registration

TAKUMI PRECISION ENGINEERING LTD·1 product·🇮🇪 Ireland

No proprietary name

FDA registration

Nelipak Healthcare Packaging·1 product·🇮🇪 Ireland

INBONE

FDA registration

WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

Duracon Knee System

FDA registration

HOWMEDICA INTERNATIONAL S. DE R.L.,·1 product·🇮🇪 Ireland

ivWatch Model 400

FDA registration

IVWATCH, LLC·1 product·🇺🇸 United States

INBONE TOTAL ANKLE SYSTEM MODEL 200347902

FDA 510(k)

FDA Class 2 ·Orthopedic

DURACON CONVERSION AND X-SMALL SYMMETRIC PATELLA WITH PERI-APATITE COATING

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer

Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer