BEUDAMED
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    SI CONTROLLER MODEL SI 500

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

    AESCULAP CRANIOFACIAL PLATE AND SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    Hospira Sapphire Sets

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 9, 2014

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·February 11, 2013

    UNIVERSAL ALTERNATE BEARING SHELL 56MM 2-HOLE WITH APICAL PLUG 41MM I.D. TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·January 13, 2011