BEUDAMED
    73 results · 35ms · Sources: EU EUDAMED, US FDA

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    BOSTON XO2 GAS PERMEABLE CONTACT LENSES

    FDA Adverse Event
    Injury ·BAUSCH & LOMB INCORPORATED·Product code HQD·February 9, 2026

    AIR OPTIX

    FDA Adverse Event
    Injury ·ALCON/NOVARTIS·Product code LPM·February 22, 2016

    Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.

    FDA Recall
    Completed ·Lens.com·Product code LPM·August 14, 2018

    Alcon Air Optix Night & Day Aqua (lotrafilcon A), breathable contact lenses, PWR - 1.50 BC 8.6 DIA 13.8, Rx, Sterile. The firm name on the label is Alcon Laboratories, Inc., Fort Worth, TX.

    FDA Enforcement
    Class II ·Completed·Lens.com·December 11, 2019

    URETEROSCOPE 6.7/8.4 FR. X 430 MM, 5°, ANGLED OCULAR, 4.2 FR. CHANNEL

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FGB·August 26, 2025

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDT·March 11, 2026

    HD CAMERA HEAD

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·December 29, 2024

    ELASTIC UV-ABSORBING SILICONE POSTERIOR CHAMBER

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·October 6, 2004

    STERRAD NX STERILIZATION SYSTEM

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·October 2, 2007

    HD CAMERA HEAD

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·June 10, 2024

    CLAREON IOL WITH THE AUTONOME DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES IRELAND LTD.·Product code HQL·December 2, 2025

    SOFPORT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code MSS·March 20, 2015

    ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code GCJ·November 9, 2022

    PROCLEAR -3.25

    FDA Adverse Event
    Malfunction ·COOPERVISION·Product code LPM·December 30, 2005

    ACRYSOF

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD.·Product code HQL·January 24, 2017

    NEPHROSCOPE ONLY FOR MIP L

    FDA Adverse Event
    Injury ·KARL STORZ SE & CO. KG·Product code FGA·April 24, 2024

    EVIS LUCERA DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDT·January 14, 2026

    EVIS LUCERA ELITE BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code EOQ·October 17, 2025

    CLAREON MONARCH IV IOL DELIVERY SYSTEM, INJECTOR

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LLC - ALCON PRECISION DEVICE·Product code MSS·March 24, 2026

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code MTA·August 20, 2008