BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    MEDTRONIC MODEL 3861 TEMPORARY SCREENING LEAD KIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    Medwell Technology Ltd Syringes, various sizes

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NeuroOne Cortical Electrode

    FDA 510(k)
    FDA Class 2 ·Neurology

    ON-Q PAIN PUMP

    FDA Adverse Event
    Injury ·I-FLOW, LLC·Product code MEB·January 8, 2013

    RSP SHOULDER

    FDA Adverse Event
    Other ·ENCORE MEDICAL, L.P.·Product code KWS·November 2, 2010

    ACUITY

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code LWP·July 3, 2014

    Exactech Equinoxe GLENOID,KEELED, CEMENTED, Mates with 38, 41, 44 head, alpha curvature, Sizes: a), Small, Item Number 314-01-02; b) Medium, Item number 314-01-03; c) Large, Item Number 314-01-04, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024

    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