BEUDAMED
    227 results · 40ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    MICROPULSE P3 DEVICE

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 15, 2025

    OCULIGHT GL LASER

    FDA Adverse Event
    Malfunction ·IRIDEX CORP.·Product code GEX·November 30, 2012

    MICROPULSE P3 DEVICE

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 23, 2025

    23-27 GAUGE; STEPPED ANGLED 45 DEGREES ENDOPROBE

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 11, 2008

    2939653-2017-00015

    FDA Adverse Event
    Injury ·November 11, 2017

    MICROPULSE P3 DEVICE

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 10, 2025

    MICROPULSE P3 DEVICE

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 10, 2025

    2939653-2018-00005

    FDA Adverse Event
    Injury ·March 21, 2018

    2939653-2018-00004

    FDA Adverse Event
    Injury ·March 21, 2018

    OCULIGHT SLX

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 21, 2016

    IQ577

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code GEX·December 28, 2016

    IRIDEX G-PROBE

    FDA Adverse Event
    Malfunction ·IRIDEX CORPORATION·Product code GEX·July 3, 2015

    IRIDEX

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·April 13, 2010

    CUST-CYLCO-G6

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·May 14, 2021

    CUST-IQ577

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·June 4, 2021

    CYCLO G6

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·May 27, 2022

    MICROPULSE P3

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·May 27, 2022

    CYCLO G6 LASER SYSTEM

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·May 27, 2022

    MICROPULSE P3

    FDA Adverse Event
    Injury ·IRIDEX CORPORATION·Product code HQF·May 4, 2022

    ENDOPROBE

    FDA Adverse Event
    Malfunction ·IRIDEX CORPORATION·Product code GEX·June 15, 2007