BEUDAMED
    10 results · 24ms · 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 ×

    Phoenix Clinical ICON

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707018896·CALIBRA 1ST MOLAR BANDS n.LL 27

    ARCUATE VERTEBRAL AUGMENTATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HOVEROUND TEKNIQUE, MODEL HD-6

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DRIVER 9735024 SOLERA 5.5/6.0 MAS CANN

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code OLO·October 30, 2019

    PELVICOL 2CM X 7 CM 1.0MM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE SCIENCE LABORATORIES·Product code FTL·June 12, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 21, 2011

    FANELLI LAPAROSCOPIC ENDOBILIARY STENT SET

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code FGE·September 11, 2008

    KYPHON KURVE BONE FILLER DEVICE 13GA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MEXICO·Product code KIH·July 14, 2020

    SLIDING MECHANISM

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTD·November 25, 2020