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    LUMENIS LTD.

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·October 16, 2024

    3004135191-2017-00010

    FDA Adverse Event
    Injury ·January 26, 2017

    VERSACUT+ TISSUE MORCELLATOR

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEI·January 26, 2017

    M22

    FDA Adverse Event
    Injury ·LUMENIS BE LTD·Product code GEX·December 29, 2021

    LUMENIS PULSE 120H

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 3, 2022

    LIGHTSHEER DUET HS/ET

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·April 28, 2022

    VERSAPULSE POWERSUITE 60W

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 3, 2022

    MOSES 200¿ D/F/L DISPOSABLE FIBER

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 3, 2022

    RESURFX

    FDA Adverse Event
    Malfunction ·LUMENIS, LTD·Product code ONG·February 20, 2017

    LIGHTSHEER XC

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·April 28, 2022

    ULTRAPULSE SURGITOUCH 120V DOMESTIC - O.R.

    FDA Adverse Event
    Injury ·LUMENIS BE LTD.·Product code GEX·June 8, 2023

    ULTRAPULSE SURGITOUCH 120V DOMESTIC - O.R.

    FDA Adverse Event
    Injury ·LUMENIS BE LTD.·Product code GEX·June 8, 2023

    LIGHTSHEER DUET

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·March 15, 2017

    POWERED LASER SURGICAL INSTRUMENT

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·July 4, 2025

    SLIMLINE

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 29, 2026

    FEMTOUCH

    FDA Adverse Event
    Malfunction ·LUMENIS LTD.·Product code GEX·October 4, 2016

    M22

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·December 12, 2016

    VERSACUT+ TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·LUMENIS, LTD.·Product code GCJ·July 1, 2015

    VERSACUT+ TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·LUMENIS, LTD.·Product code GCJ·July 1, 2015

    LASER MICROMANIPULATOR JOYSTICK

    FDA Adverse Event
    Malfunction ·LUMENIS LTD·Product code GEX·August 27, 2015