2,029 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·March 29, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·February 1, 2023
ALCON, ENGAUGE
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQF·February 2, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·February 15, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·March 2, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·March 23, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·February 21, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·February 24, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·March 23, 2023
PUREPOINT LASER
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQF·September 20, 2024
LASER PROBE
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQF·July 2, 2002
UNK
FDA Adverse Event
Injury
·UNK·Product code HQF·August 14, 2002
HGM INC
FDA Adverse Event
Injury
·HGM INC (LUMENIS)·Product code HQF·July 2, 2002
NOVUS OMNI DUAL 3 PHASE
FDA Adverse Event
Injury
·LUMENIS·Product code HQF·September 27, 2002
OPHTHALAS 532 LASER
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQF·September 27, 2002
VISEX LASER
FDA Adverse Event
VISION SCULPING·Product code HQF·October 5, 1995
EXIMER LASER FOR PRK & PTK
FDA Adverse Event
Malfunction
·UNKNOWN·Product code HQF·October 5, 1995
TEUTON
FDA Adverse Event
VISX, INC.·Product code HQF·October 5, 1995
SHARPLAN SIDEFIRE LASER
FDA Adverse Event
Malfunction
·MYRIADLASE, INC.·Product code HQF·October 25, 1995
LASIK EYE SURGERY
FDA Adverse Event
Injury
·Product code HQF·November 4, 2007