BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    GORE-TEX DUALMESH BIOMATERIAL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    POGO SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Avenir Complete Hip System, Size 0 Coxa Vara

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DESARA

    FDA Adverse Event
    Injury ·CALDERA MEDICAL, INC.·Product code FTL·February 28, 2013

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014

    ASKU

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA INC.·Product code DTE·February 15, 2011