BEUDAMED
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    QUALICHECK 2

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994238849·ROD 7894110 STRAIGHT 5.5MM X 110MM PEEK

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690197621·AK3 PS-C Insert Trial Size 1, 10mm

    ANTENSE ANTI-TENSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Neurology

    XTRACETEZE SURGICAL SKIN STAPLE REMOVER 2001

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

    THAL-QUICK CHEST TUBE TRAY

    FDA Adverse Event
    Injury ·COOK, INC.·Product code KDQ·June 20, 2014

    AC POWER MODULE

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·November 4, 2010

    AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM - ANTERIOR

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·December 27, 2012