Velofix Interbody Fusion System

FDA registration

CG MedTech USA, Inc.·2 products·🇺🇸 United States

Velofix Interbody Fusion System

FDA registration

CG MedTech Co., Ltd.·2 products·🇰🇷 South Korea

VELOXTM INTERBODY FUSION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

ATTIC DEFECT PLATE 14 MM DIAMETER POROUS HYDROXYLAPATITE

FDA UDI

Gyrus Acmi, Inc.·00821925012301·ATTIC DEFECT PLATE 14 MM DIAMETER POROUS HYDROX...

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

AESCULAP, INC.

FDA registration

AESCULAP, INC.·1 product·🇺🇸 United States

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

Optilite® Alpha-2-Macroglobulin Kit

FDA registration

The Binding Site Group Ltd.·1 product·🇬🇧 United Kingdom

s-max (D1611 Aviation)

FDA registration

AAT Alber Antriebstechnik GmbH·1 product·🇩🇪 Germany

3M Deutschland GmbH

FDA registration

3M Deutschland GmbH·1 product·🇩🇪 Germany

Optilite® Alpha-2-Macroglobulin Kit

FDA registration

THE BINDING SITE·1 product·🇬🇧 United Kingdom

3M Deutschland GmbH

FDA registration

3M Deutschland GmbH·1 product·🇩🇪 Germany

CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM

FDA 510(k)

FDA Class 2 ·Neurology

BIOSPINE VBR SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

Plate, Cranioplasty, Preformed, Non-Alterable

FDA classification

FDA Class 2 ·Plate, Cranioplasty, Preformed, Non-Alterable

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device