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

    MODIFICATION TO SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REMVIEW SLEEP RECORDER, MODEL 320

    FDA 510(k)
    FDA Class 2 ·Neurology

    DIOMED 15 PLUS AND DIOMED 30PLUS LASERS

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

    Fastener, Fixation, Nondegradable, Soft Tissue

    FDA classification
    FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

    Device, Sleep Assessment

    FDA classification
    FDA Class 2 ·Device, Sleep Assessment

    Powered Laser Surgical Instrument

    FDA classification
    FDA Class 2 ·Powered Laser Surgical Instrument