263 results · 44ms · Sources: EU EUDAMED, US FDA

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LUMENIS LTD

Manufacturer
🇮🇱 Israel·2 Importers

VERSACUT

FDA Adverse Event
Other ·LUMENIS·Product code GCJ·March 14, 2013

EPILIGHT

FDA Adverse Event
Other ·LUMENIS LTD·Product code GEX·January 8, 2007

EPILIGHT

FDA Adverse Event
Injury ·LUMENIS, (ISRAEL)·Product code GEX·August 5, 2005

SLIMLINE 550 FIBER

FDA Adverse Event
Injury ·LUMENIS, LTD.·Product code GEX·May 7, 2014

LUMENIS ONE

FDA Adverse Event
Injury ·LUMENIS LTD·Product code GEX·March 16, 2007

SLIM LINE SIS 365

FDA Adverse Event
Injury ·LUMENIS, LTD.·Product code GEX·August 28, 2013

LUMENISONE

FDA Adverse Event
Injury ·LUMENIS LTD.·Product code GEX·March 13, 2007

LIGHTSHEER XC

FDA Adverse Event
Injury ·RH USA, INC.·Product code GEX·October 31, 2012

SPLENDOR X

FDA Adverse Event
Injury ·BIOS S.R.L·Product code GEX·June 13, 2025

SLIMLINE 550

FDA Adverse Event
Injury ·LUMENIS, LTD.·Product code GEX·August 15, 2013

QUANTUM

FDA Adverse Event
Injury ·LUMENIS, INC.·Product code GEX·May 11, 2006

TRILIFT

FDA Adverse Event
Injury ·POLLOGEN LTD·Product code NGX·September 23, 2023

SLIMLINE FIBER

FDA Adverse Event
Injury ·LUMENIS LTD.·Product code GEX·December 4, 2017

SELECTA DUET

FDA Adverse Event
Other ·ELLEX·Product code GEX·January 9, 2007

LIGHTSHEER DUET

FDA Adverse Event
Injury ·RH USA, INC.·Product code GEX·January 26, 2011

SPLENDOR X

FDA Adverse Event
Injury ·BIOS SRL·Product code GEX·June 9, 2025

SPLENDOR X

FDA Adverse Event
Injury ·BIOS SRL·Product code GEX·June 9, 2025

LIGHTSHEER DUET

FDA Adverse Event
Injury ·LUMENIS INC.·Product code GEX·January 19, 2012

LUMENIS ONE

FDA Adverse Event
Injury ·LUMENIS LTD·Product code GEX·November 30, 2011