BEUDAMED
    16 results · 30ms · 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 ×

    UNIVERS VAULTLOCK GLENOID, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KWS·January 5, 2026

    UNIVERS VAULTLOCK GLENOID, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KWS·October 4, 2021

    MICROPUNCTURE TRANSITIONLESS ACCESS SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·November 30, 2010

    COMMUNICATOR

    FDA Adverse Event
    Malfunction ·EXTERNAL MANUFACTURER·Product code LWS·January 11, 2013

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·HEARTWARE, INC·Product code DSQ·July 2, 2014

    UNIVERS VAULTLOCK GLENOID, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code KWS·November 27, 2024

    ECLIPSE CAGE SCREW L, 40MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·June 6, 2025

    ECLIPSE TRUNION 47MM, SLOTTED, TPS CAP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·June 6, 2025

    ARTHREX ECLIPSE HUMERAL HEAD, 47/18

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·May 9, 2025

    UNIVERS APEX HUMERAL STEM, 12MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·May 14, 2020

    USP II HUMERAL HEAD 50/19

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·May 14, 2020

    UNIVERS VAULTLOCK GLENOID, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·May 14, 2020

    UNIVERS VAULTLOCK GLENOID, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·June 6, 2025

    UNIVERS VAULTLOCK GLENOID, LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 5, 2024

    UNIVERS II HUMERAL HEAD 56/22

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 5, 2024

    UNIVERS APEX HUMERAL STEM, 11MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·December 5, 2024