BEUDAMED
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    HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Arthrex®

    FDA UDI
    ARTHREX, INC.·10888867127200·.045" GUIDE WIRE TROCAR, THREADED

    ESCHMANN DILATION CATHETER

    FDA 510(k)

    NEUROMOD COMPLEMENT #7724 DUAL CHANNEL

    FDA 510(k)
    FDA Class 2 ·Neurology

    .045" GUIDE WIRE TROCAR, THREADED

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NBH·February 26, 2020

    G-WIRE W/TRCR TIP, THDD, 062"X9.25"

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code LXH·February 26, 2020

    .045" GUIDE WIRE TROCAR, THREADED

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code NBH·June 2, 2025

    .045" GUIDE WIRE TROCAR, THREADED

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code NBH·September 19, 2018

    TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 19, 2010

    TRANSCONNECTOR

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWQ·December 14, 2012

    9MM FLUTED BALL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GFF·November 27, 2013