BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    MYOTRAC

    FDA 510(k)
    FDA Class 2 ·Neurology

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517310828·Archon Screw, 4.0x16mm S.T. Variable

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799006127·

    Sapphire Dorsal Comfort Fit

    FDA 510(k)
    FDA Class 2 ·Dental

    PALOMAR ASPIRE LASER PLATFORM

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

    NC QUANTUM APEX PTCA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·October 25, 2010

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 18, 2014

    LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 20, 2012

    KORA

    FDA Adverse Event
    Malfunction ·MICROPORT CRM S.R.L.·Product code LWP·November 6, 2024

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021