BEUDAMED
    6 results · 77ms · 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.
    Filters FDA Adverse Event ×

    VILEX IMPLANT

    FDA Adverse Event
    Malfunction ·VILEX IN TENNESSEE, INC.·Product code KWD·November 15, 2017

    VILEX 8.0MM CANNULATED SCREW

    FDA Adverse Event
    Injury ·VILEX IN TENNESSEE, INC.·Product code HWC·July 22, 2011

    VILEX 3.0MM CANNULATED LAG SCREW

    FDA Adverse Event
    Malfunction ·VILEX IN TENNESSEE, INC.·Product code HWC·September 19, 2011

    VILEX 3.0MM DUAL THREAD "HEADLESS" SCREW

    FDA Adverse Event
    Malfunction ·VILEX IN TENNESSEE, INC·Product code JDW·November 15, 2012

    VILEX HEMI IMPLANT

    FDA Adverse Event
    Malfunction ·VILEX IN TENNESSEE, INC.·Product code KWD·February 27, 2018

    VILEX DRILL BIT

    FDA Adverse Event
    Malfunction ·VILEX IN TENNESEE, INC.·Product code GFF·June 2, 2016