BEUDAMED
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    4-LEAD IRRIGATION SET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690188285·NOTCHED POSTERIOR AUGMENT TRIAL REVISION FEMUR ...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690128922·Femoral Augment, Notched Posterior, Size 2+, 10mm

    ID-RING

    FDA UDI
    DiaDent Group International·08806383525541·Used for color coding files

    STAR TOTAL ANKLE REPLACEMENT

    FDA Adverse Event
    Injury ·SMALL BONE INNOVATIONS, INC.·Product code NTG·May 20, 2014

    ABACUS (TM) SPACER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CASHMERE POWDER FREE NITRILE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MEDTRONIC MINIMED PARADIGM SILHOUETTE INSULIN INFUSION

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code FPA·December 25, 2010

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code KPE·July 17, 2014

    DEXTRUS 4135

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·December 27, 2012