89 results
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49ms
·
Sources: EU EUDAMED, US FDA
RH USA, INC.
FDA registration
RH USA, INC.·5 products·🇺🇸 United States
Lumenis brand LightSheer Pulsed Diode Array Laser System; All serial numbers; Manufactured by RH USA, Inc., 201 Lindbergh Avenue, Livermore, California 94551
FDA Recall
Terminated
·Lumenis Inc.·Product code GEX·February 9, 2006
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·June 17, 2014
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·April 18, 2014
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·February 19, 2010
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·February 9, 2010
LIGHTSHEER DUET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·March 4, 2010
ULTRAPULSE ENCORE
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·February 12, 2010
LIGHTSHEER DUET
FDA Adverse Event
Other
·RH USA, INC.·Product code GEX·January 8, 2010
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·January 21, 2010
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC·Product code GEX·May 27, 2010
LIGHTSHEER DUET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·April 23, 2010
LIGHTSHEER XC
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·May 20, 2010
LIGHTSHEER ET
FDA Adverse Event
Other
·RH USA, INC.·Product code GEX·June 21, 2010
LIGHTSHEER DUET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·August 3, 2015
LIGHTSHEER EC
FDA Adverse Event
RH USA, INC.·Product code GEX·June 9, 2014
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·April 9, 2014
LIGHTSHEER DUET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·October 22, 2014
LIGHTSHEER ET
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·May 2, 2012
LIGHTSHEER SC
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·May 16, 2012