Kinemax+ Knee

FDA registration

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

KINEMAX PLUS ALL PLASTIC TIBIAL COMPONENT

FDA 510(k)

FDA Class 2 ·Orthopedic

De Soutter Medical

FDA UDI

DE SOUTTER MEDICAL LIMITED·05051471123267·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 100mm

Zimmer Patient Specific Instruments

FDA registration

Materialise USA, LLC.·2 products·🇺🇸 United States

TECHNOLAS PERFECT VISION GMBH

FDA registration

TECHNOLAS PERFECT VISION GMBH·1 product·🇩🇪 Germany

Zimmer Patient Specific Instruments

FDA registration

Materialise Ukraine, Rep. office·2 products·🇺🇦 Ukraine

Zimmer Patient Specific Instruments

FDA registration

MATERIALISE N.V.·2 products·🇧🇪 Belgium

Bausch & Lomb Incorporated

FDA registration

Bausch & Lomb Incorporated·1 product·🇺🇸 United States

Zimmer Patient Specific Instruments

FDA registration

Materialise Sdn Bhd·2 products·🇲🇾 Malaysia

AlloMap Heart

FDA registration

CareDx, Inc.·1 product·🇺🇸 United States

ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

HANSATOME EXCELLUS MICROKERATOME

FDA 510(k)

FDA Class 1 ·Ophthalmic

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

FDA classification

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

Keratome, Ac-Powered

FDA classification

FDA Class 1 ·Keratome, Ac-Powered