BEUDAMED
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    SUTURE PLACEMENT DEVICE AND ACCESSORIES

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

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981531·anteriors; shade BL4; mould IM4

    SpineEX Sagittae Lateral Lumbar Interbody Fusion Devices

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AOC SOLUBLE IMPLANT MATERIAL

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 27, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·August 5, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·January 31, 2011