BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Genesys Spine 3DP Lumbar Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HRK-63-16 KNEE ARRAY COIL, HRK-127-16 KNEE ARRAY COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    TWISTER SIDE FIRE OPTICAL FIBER DELIVERY SYSTEM

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

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Coil, Magnetic Resonance, Specialty

    FDA classification
    FDA Class 2 ·Coil, Magnetic Resonance, Specialty

    Powered Laser Surgical Instrument

    FDA classification
    FDA Class 2 ·Powered Laser Surgical Instrument