BEUDAMED
    16 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 ×

    STERN ERA ALIGNMENT CORRECTION IMPLANT ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    Bosworth SuperEBA

    FDA UDI
    Harry J Bosworth Company·H66809210101·6.5 ml ZOE Cement Liquid

    PAQ.210X280X350*31*SCH.AT-60

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763009474·

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690115373·Retaining Bolt PS or PS-C Insert, Modular Tibia...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690192954·CR Tibia Tray Slap Hammer Adapter

    ZAVATION

    FDA UDI
    Zavation LLC·00842166152649·WHITNEY 14mmx16mm , 10deg , 10mm

    SOLAR SHIELD

    FDA UDI
    FGX INTERNATIONAL INC.·00887661481962·

    SOLAR SHIELD

    FDA UDI
    FGX INTERNATIONAL INC.·00031568481963·

    SOLAR SHIELD

    FDA UDI
    FGX INTERNATIONAL INC.·00887661344878·

    SOLAR SHIELD

    FDA UDI
    FGX INTERNATIONAL INC.·00883019088630·

    SOLAR SHIELD

    FDA UDI
    FGX INTERNATIONAL INC.·00846150006444·

    M7/M7T DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSE

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

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 17, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·December 9, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2014