BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAVERMAP SURGICAL AID

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VISTAKON (METHAFILCON A) CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Stimulator, Nerve

    FDA classification
    FDA Class 2 ·Stimulator, Nerve

    Lenses, Soft Contact, Daily Wear

    FDA classification
    FDA Class 2 ·Lenses, Soft Contact, Daily Wear