50 results
·
71ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
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