BEUDAMED
    7 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    KXO-80C/80D

    FDA 510(k)
    FDA Class 1 ·Radiology

    LIGAMENTOTAXOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    METAL TRANSCEND ARTICULATION SYSTEM

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    TITAN TOUCH SCRO ZERO ANG 22CM

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·May 22, 2018

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code LKK·January 9, 2013

    GORE TAG THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·November 15, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 1, 2014