BEUDAMED
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    Q-FIX ULTRA All-Suture Anchor

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Blade Scalpel

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113462·SCLEROTOME BLADE #57 (BX/5)

    LAG SCREW, TI GAMMA3 10.5X95MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 25, 2012

    MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM

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

    FORA DIAMOND NEXUS MINI INFRARED FOREHEAD THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ASR UNI FEMORAL IMPL SIZE 41

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 2, 2011

    42 ML CAN SAF

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD. (CONTRACT MANUFACTURER FOR HOSPIRA, INC.)·Product code GCX·September 24, 2014

    ANEURX

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 18, 2013