BEUDAMED
    8 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 ×

    ARCOS CON SZ C STD 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 20, 2026

    G7 SCREW 6.5MM X 30MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·May 20, 2026

    G7 OSSEOTI MULTIHOLE 58MM G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 20, 2026

    ARCOS 15X150MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 20, 2026

    DELTA CERAMIC FEM HD 36/-3MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·May 27, 2026

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 29, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 13, 2011

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 8, 2013