BEUDAMED
    10 results · 19ms · 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 ×

    CENTURION CIRCLAMP

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

    TRITANIUM NON-MODULAR SHELL & X3 ALL-POLY INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUAD IV CUSTOM IMPRESSION TRAY

    FDA 510(k)
    FDA Class 1 ·Dental

    2124215-2010-16366

    FDA Adverse Event
    Injury ·GUIDANT PUERTO RICO BV·Product code ODL·August 16, 2010

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 4, 2014

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC. (FORMERLY BIOFORM MEDICAL, INC.)·Product code LNM·October 29, 2010

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 21, 2012

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·September 6, 2023

    ONYX

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·September 6, 2023

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·August 12, 2025