BEUDAMED
    3 results · 21ms · 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 ×

    UNIVERSAL OSCILLATING SAW ATTACHMENT

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A.·Product code GFA·April 1, 2014

    UNKNOWN SOFT CONTACT LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code LPL·October 31, 2012

    IMPLANTIUM

    FDA Adverse Event
    Injury ·DENTIUM USA·Product code DZE·August 26, 2010