BEUDAMED
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    AURA ICP MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100837·FLIERINGA FIXATION RING 22MM

    ENCODE PATIENT SPECIFIC ABUTMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    PREFILLED CATHETER INFLATION SYRINGE

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

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2013

    COBAS 6000 C501MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·September 19, 2008

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 15, 2011