BEUDAMED
    6 results · 18ms · 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 ×

    THE EXPANDACELL SINUS PACK

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    IONOBOND

    FDA 510(k)
    FDA Class 2 ·Dental

    MODEL 6984M LEAD EXTENDER KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTRAMEDULLARY SKELETAL KINETIC DISTRACTOR

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code HSB·January 3, 2013

    POSEY KEEPSAFE FALL MONITOR

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·December 16, 2010

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITJ·July 15, 2014