BEUDAMED
    10 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.

    iLet® Dosing Decision Software

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VISION XR

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975024831·Vision XR DB-57 D-Speed Double Intraoral Film

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111306518·SKLIT XD DERF NH SERR 4.75"

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·November 10, 2003

    BIORCI SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNIMED SURGICAL COATED ELECTROSURGICAL ELECTRODES

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

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 14, 2008

    DXTEND STAND PE CUP D42 +9MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.·Product code KWS·August 18, 2011

    PELVICOL (BARD) 8CM X 12CM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·July 8, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025