50 results · 71ms · Sources: EU EUDAMED, US FDA

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LASER PERIPHERALS LLC DBLF-100

FDA Adverse Event
Injury ·LASER PERIPHERALS LLC·Product code GEX·May 9, 2014

HOLMIUM BARE LASER FIBER

FDA Adverse Event
LASER PERIPHERALS, LLC·Product code GEX·January 14, 2014

ENDOBEAM¿ HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code GEX·February 7, 2018

ENDOBEAM HOLMIUM LASER FIBERS

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC·Product code GEX·October 17, 2014

ENDOBEAM HOLMIUM LASER FIBERS

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC·Product code GEX·December 19, 2014

940U LASER FIBER PL

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC.·Product code GEX·August 22, 2024

POWERED LASER SURGICAL INSTRUMENT

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC.·Product code GEX·May 18, 2026

ENDOBEAM, HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC·Product code GEX·January 17, 2013

ENDOBEAM HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC·Product code GEX·January 17, 2013

ENDOBEAM HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC·Product code GEX·January 17, 2013

*

FDA Adverse Event
Malfunction ·LASER PERIPHERALS LLC·Product code GEX·December 14, 2009

HTB-272-PL

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·December 21, 2018

LASER PERIPHERALS SCATTERFREE FIBERS

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·September 28, 2020

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·March 7, 2011

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025

RBLF LASER FIBER

FDA Adverse Event
Injury ·LASER PERIPHERALS, LLC·Product code LNK·March 10, 2006

LASER PERIPHERALS DIODE LASER FIBER

FDA Adverse Event
Injury ·LASER PERIPHERALS LLC.·Product code GEX·October 14, 2005

8000229

FDA Adverse Event
Malfunction ·LASER PERIPHERALS, LLC·Product code GEX·August 7, 2025