BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    PERSONAL BACK WITH FIP KIT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    SUCTION TUBE

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

    MARTIN LAMINAR OSTEOSYNTHESIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    THERAKOS XTS PHOTOPHERESIS SYSTEM

    FDA Adverse Event
    Malfunction ·THERAKOS, INC.·Product code LNR·May 19, 2014

    NEW LIGASURE 5MM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·November 5, 2010

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·December 20, 2012

    BIOMET StageOne Knee Femoral Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 432170.

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