BEUDAMED
    6 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 Regulation: Us FDA ×

    FOCUS MODEL 795 UNIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    CERAMENT BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Destino Reach

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATTAIN ABILITY PLUS

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 23, 2014