BEUDAMED
    8 results · 20ms · 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 ×

    pRESET Thrombectomy Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    S2 Pigment Removal System

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

    LENSTEC LC INJECTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 14, 2025

    ROTABLATOR CONSOLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code MCX·November 6, 2008

    BIOTENE ORALBALANCE GEL

    FDA Adverse Event
    Other ·LACLEDE, INC.·Product code LFD·August 9, 2011

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 12, 2013

    200 MICRON TFL SINGLE USE FIBER

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code GEX·October 5, 2022