BEUDAMED
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    DA VINCI FIREFLY IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    M2a-Magnum™

    FDA UDI
    Biomet Orthopedics, LLC·00887868474347·

    MAGNUM INSTRUMENTATION

    FDA UDI
    Biomet Uk Ltd·05019279440375·

    DA VINCI FLUORESCENCE IMAGING VISION SYSTEM, MODEL FF 100

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    IMALUX OCT PROBE GUIDE

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

    Widex

    FDA UDI
    Widex A/S·05706069812572·Widex EVOKE E-PA (Shocking pink ) 440, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069886566·WIDEX MOMENT MRB0 (Shocking pink ) 440, RIC 10

    BELLAFILL DERMAL FILLER

    FDA Adverse Event
    Injury ·SUNEVA MEDICAL, INC.·Product code LMH·July 12, 2019

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·June 3, 2013

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code BTS·June 21, 2011

    FOLFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 3, 2014

    SUPERSHEATH

    FDA Adverse Event
    Malfunction ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022

    SUPERSHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018

    SUPERSHEATH

    FDA Adverse Event
    Malfunction ·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    SUPER SHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·April 28, 2020

    SUPERSHEATH

    FDA Adverse Event
    Injury ·TOGO MEDIKIT CO. LTD.·Product code DRE·April 11, 2017