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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