1,061 results
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64ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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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
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
M22
FDA Adverse Event
Injury
·LUMENIS, LTD.·Product code GEX·December 12, 2016
VASCULIGHT SR
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·March 16, 2012
LIGHTSHEER DUET
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·February 16, 2012
VERSACUT MORCELLATOR
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GCJ·February 27, 2012
LIGHTSHEER DUET
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·March 30, 2012
M22
FDA Adverse Event
Injury
·LUMENIS, LTD.·Product code GEX·June 18, 2014