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