BEUDAMED
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    LAMINARIA TENT

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

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198567·AK3 Ultra Insert Trial Size 2, 20mm

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G586N8922200·brand tendon tunnelling forceps, 1x2 teeth, cur...

    ReliOn Premier Classic Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VANCE KIDNEY BIOPSY BRUSHES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    89-2220 T & A VALUE SET

    FDA Adverse Event
    Other ·DEROYAL INC.·Product code DTL·May 8, 2001

    SYNERGY?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 24, 2014

    PRECISE PRO RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIM·January 2, 2013

    NEXGEN LPS ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 26, 2010

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020