BEUDAMED
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    GAUZE SPONGE, X-RAY DETECTABLE

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

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867386464·Cortical Screw, 2.7 mm x 8 mm

    SYSTEM, ECHO, PULSED ULTRASONIC DIAG.

    FDA 510(k)
    FDA Class 2 ·Radiology

    PARAMAX CALCIUM REAGENT-GLUTAMY-TRANS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EPOLY 36MM RNGLC LNR HW SZ25

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·June 19, 2014

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·October 21, 2010

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 20, 2012