Novostitch Plus

FDA registration

CETERIX ORTHOPAEDICS, INC·1 product·🇺🇸 United States

NovoStitch Meniscal Repair Cartridge, size 2-0

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

NovoStitch Plus Meniscal Repair System

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Suture, Nonabsorbable, Synthetic, Polyethylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polyethylene

Wagner SL Revision Stem Lateral

FDA registration

ZIMMER GMBH·1 product·🇨🇭 Switzerland

ZimmerGmbH8803 (DK) - Wagner SL Revision®

FDA registration

Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

Fortiva¿ porcine dermis, Tutoplast® porcine dermis

FDA registration

RTI Surgical, Inc. (dba RTI Biologics, Inc.)·1 product·🇺🇸 United States

Tutoplast® porcine dermis

FDA registration

Sterigenics Belgium Fleurus SA·1 product·🇧🇪 Belgium

Wagner SL Revision Stem Lateral

FDA registration

Biomet Global Supply Chain Center B.V.·1 product·🇳🇱 Netherlands

Fortiva¿ porcine dermis, Tutoplast® porcine dermis

FDA registration

Tutogen Medical GmBH·1 product·🇩🇪 Germany

Biomet Microfixation OmniMax MMF System

FDA registration

Changzhou Biomet Medical Devices Co., Ltd.·2 products·🇨🇳 China

PROLENE Polypropylene Suture

FDA registration

ETHICON, LLC·1 product·🇺🇸 United States

Attain Hybrid Guide Wire

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

E.M Adams co, inc.

FDA UDI

E.M. ADAMS, INC.·18100013402019·SINGLE INSTRUMENT

E.M Adams co, inc.

FDA UDI

E.M. ADAMS, INC.·10840200302019·SINGLE INSTRUMENT

WAGNER SL REVISION STEM LATERAL

FDA 510(k)

FDA Class 2 ·Orthopedic

PRUITT CAROTID KIT

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Intravascular Occluding, Temporary

FDA classification

FDA Class 2 ·Catheter, Intravascular Occluding, Temporary

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented