BEUDAMED
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    AUTOMATED BIOPSY DEVICE, MODIFICATION

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909138152·REVELATION DIAMOND 885-014C - 5 PACK

    MEDRAD QWIK-FIT SYRINGE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESSCAN

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·November 26, 2010

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·July 3, 2014

    DIGITAL RADIOGRAPHY CXDI-70C WIRELESS

    FDA Adverse Event
    Malfunction ·CANON, INC.·Product code MQB·September 25, 2012