BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    Pro-Link® Ti Stand-Alone Cervical Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015

    COMPREHENSIVE REVERSE SHOULDER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILJETR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    COVIDIEN

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH, INC.·Product code KNT·July 24, 2024

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·January 28, 2026

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·April 26, 2022

    INSERT-HANDLE RADIOLUC F/PFNA

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code LXH·June 20, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 15, 2014

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 5, 2011

    COPELAND THN SHL COCR/HA HUMS3

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·August 28, 2025