BEUDAMED
    21 results · 42ms · Sources: EU EUDAMED, US FDA

    SPINE WAVE, INC.

    FDA registration
    SPINE WAVE, INC.·1 product·🇺🇸 United States

    SpineWave3277 (NR,WH) - StaXx Lordotic XD

    FDA registration
    ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

    SpineWave3277 (NR,WH) - StaXx Lordotic XD

    FDA registration
    ISOMEDIX OPERATIONS INC.·1 product·🇺🇸 United States

    PPD MEDITECH, DIV. OF INDUSTRIES PPD INC.

    FDA registration
    PPD MEDITECH, DIV. OF INDUSTRIES PPD INC.·1 product·🇨🇦 Canada

    STAXX XD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SFAM-Surgiform

    FDA registration
    Eurofins Infinity Laboratory Group Inc.·1 product·🇺🇸 United States

    PIVOTAL HEALTH SOLUTIONS

    FDA registration
    PIVOTAL HEALTH SOLUTIONS·1 product·🇺🇸 United States

    SFAM 3-D

    FDA registration
    SURGICAL TECHNOLOGY LABORATORIES INC.·1 product·🇺🇸 United States

    Shang Ring

    FDA registration
    Wuhu Snnda Medical Treatment Appliance Technology Co. Ltd.·1 product·🇨🇳 China

    Spinal Vertebral Body Replacement Device

    FDA classification
    FDA Class 2 ·Spinal Vertebral Body Replacement Device

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012702·CERAMAX Ceramic Insert NEUTRAL 58mm OD 28mm ID

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012696·CERAMAX Ceramic Insert NEUTRAL 56mm OD 28mm ID

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012689·CERAMAX Ceramic Insert NEUTRAL 54mm OD 28mm ID

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012672·CERAMAX Ceramic Insert NEUTRAL 52mm OD 28mm ID

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012719·CERAMAX Ceramic Insert NEUTRAL 60mm OD 28mm ID

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012658·CERAMAX Ceramic Insert NEUTRAL 48mm OD 28mm ID

    CERAMAX

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295012665·CERAMAX Ceramic Insert NEUTRAL 50mm OD 28mm ID

    SURGIFORM AUGMENTATION MATERIAL (S.F.A.M.)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DECOMPRESSION OF CHOICE AND NEURO DECOMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

    FDA classification
    FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction