BEUDAMED
    7 results · 26ms · 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.

    ACUFEX STERILE DRILLS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CO2 FRACTIONAL LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MODIFICATION TO FORTITUDE CEMENT RESTRICTOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MENTOR SMOOTH ROUND MODERATE PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·November 13, 2025

    FRESENIUS 2008K

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 24, 2014

    PERMOBIL C500 CORPUS

    FDA Adverse Event
    Malfunction ·PERMOBIL, AB·Product code ITI·December 10, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·January 28, 2013