BEUDAMED
    5 results · 22ms · 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 ×

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 2, 2014

    SOLETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·November 21, 2012

    COULTER ® LH750

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·September 23, 2010

    TIBIAL INSERT FB SZ 2 RT 6MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSN·May 29, 2024

    MENTOR TISSUE EXPANDER

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·February 4, 2019