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 ×

    GLENROE ORTHO SEPS

    FDA 510(k)
    FDA Class 1 ·Dental

    AIGIS-INLAY

    FDA 510(k)
    FDA Class 2 ·Dental

    SINGLE LUMEN CATHETER KITS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    135 DEG AIMING ARM F/PROXIMAL FEMORAL NAIL INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code FZX·January 22, 2013

    CONSULTA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·December 14, 2010

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014