BEUDAMED
    7 results · 27ms · 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.

    ELECTRIC MOUTH MIRROR

    FDA 510(k)
    FDA Class 1 ·Dental

    INBODY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Patient Examination Gloves

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARM & HAMMER SPINBRUSH PROCLEAN

    FDA Adverse Event
    Malfunction ·Product code JEQ·May 1, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 13, 2012

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    EV3 Pipeline Flex Embolization Device with Flex Shield Technology

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021