BEUDAMED
    4 results · 29ms · 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 ×

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 20, 2013

    TAPERLOC MICROPLASTY FEMORAL 11MM X 107.5MM POROUS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBL·March 10, 2011

    HYLAMER 10D 60 OR 72ODX32ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·March 13, 2008

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·December 16, 2020