BEUDAMED
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    MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)

    FDA 510(k)
    FDA Class 1 ·Dental

    ULTRASOUND SCANNER XL

    FDA 510(k)
    FDA Class 2 ·Radiology

    EGNELL-LACT B BATTERY-OPERATED BREAST PUMP

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

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 10, 2014

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 7, 2010

    RSP SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code KWS·December 5, 2012

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021