BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    MOTOR RISER TOLIT LIFT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517658883·Archon Screw, Ø4.5x14mm Self Drill Vari

    Sterling Supreme Diode Laser

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

    ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·April 30, 2014

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·June 21, 2007

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 10, 2012

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025