BEUDAMED
    8 results · 17ms · Sources: EU EUDAMED, US FDA

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    CUTO(TM) TISSUE MORCELLATION SYSTEM

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

    PERIMETER INTERBODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BLACKSTONE SURGICAL TITANIUM MESH SYSTEM ANGLED END RINGS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DORNIER

    FDA Adverse Event
    Death ·DORNIER·Product code LNS·August 31, 1993

    GENERATOR PULSAR2

    FDA Adverse Event
    Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code GEI·January 29, 2013

    HYDROGEL COATED PERCUFLEX(R) DRAINAGE CATHETERS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·December 20, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 14, 2014

    Exactech Equinoxe Humeral Liner: Item Numbers: a) 320-40-00, b) 320-40-03; Shoulder Arthroplasty

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