2,029 results · 22ms · Sources: EU EUDAMED, 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