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.

    IMPLANT DRIVERS AND TIPS

    FDA 510(k)
    FDA Class 2 ·Dental

    SOLVENEX I-0

    FDA 510(k)
    FDA Class 2 ·Dental

    MyoSure XL Tissue Removal Device for Fluent

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·April 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 26, 2007

    THYSSENKRUPP ACCESS (WHEEL-O-VATOR)

    FDA Adverse Event
    Injury ·THYSSENKRUPP ACCESS·Product code ING·September 14, 2012