BEUDAMED
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    JO PREMIUM PERSONAL LUBRICANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ELPHA, MODELS II 500, II 1000, II 2000, II 3000 AND E80

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CUTERA QSWITCH LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 1, 2014

    CODMAN EXTERNAL DRAINAGE SYSTEM III

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code JXG·May 29, 2013

    MEGA NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 17, 2011