BEUDAMED
    7 results · 25ms · 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.

    CODE-A-WELL SERIES 1-600, 1-625

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ALLY™ Facet Screws

    FDA 510(k)
    FDA Unclassified ·Unknown

    NITINOL LOCKING INCUDO-STAPEDIAL JOINT, ANGULAR PISTON, PISTON, MALLEUS PISTON, PORP AND FOOTPLATE SHOE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    REVEAL LINQ

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DSI·June 10, 2014

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 9, 2010

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·December 10, 2012

    COBAS 6000 C (501) MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 29, 2025