BEUDAMED
    4 results · 35ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    AMENDIA GUIDEWIRE

    FDA Adverse Event
    Malfunction ·AMENDIA, INC.·Product code DQX·January 12, 2011

    SCREWS

    FDA Adverse Event
    Malfunction ·AMENDIA, INC.·Product code MRW·February 17, 2016

    MAKO IMPLANT

    FDA Adverse Event
    Injury ·AMENDIA, INC.·Product code HWC·July 6, 2010

    SAVANNAH-T PEDICLE SCREW SYSTEM

    FDA Adverse Event
    AMENDIA / SPINAL ELEMENTS, INC.·Product code NKB·April 30, 2019