BEUDAMED
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    SILASTIC ILEAL RESERVOIR CATHETER

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110683·LUER ADAPTOR FOR IRRIGATION

    MiniMed Quick-serter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TURKOM-CERA

    FDA 510(k)
    FDA Class 2 ·Dental

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 21, 2014

    WALLFLEX ¿ DUODENAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MUM·September 26, 2012

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·July 14, 2010

    BIPLATE SCHAEDLER/SCHAED KV 5% SB 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·June 25, 2021

    BD BBL¿ SCHAEDLER K-V AGAR WITH 5% SHEEP BLOOD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·August 2, 2021

    BIPLATE SCHAEDLER/SCHAED KV 5% SB 20

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·July 1, 2021

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025

    PROPONENT DR Pacemaker, SL (Model Number L201), (VDD) SL (Model Number L209), SL MRI (Model Number L211), EL (Model Number L221), and EL MRI (Model Number L231).

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·January 22, 2025