BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    ACU-SIZER(TM)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    G-FORCE GEN 2 SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ULTRALIGHT II ND:YAG LASER SYSTEM

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

    CELOFTAL

    FDA Adverse Event
    Injury ·ALCON - BELGIUM/ ALCON N.V.·Product code LZP·June 30, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·December 22, 2010

    ARTHREX

    FDA Adverse Event
    Malfunction ·ARTHREX·Product code LXH·October 17, 2006