712 results
·
24ms
·
Sources: EU EUDAMED, US FDA
oniris
Manufacturer
🇫🇷 France
ONIRIS
FDA registration
ONIRIS·1 product·🇫🇷 France
Oniris; Oniris Plus
FDA 510(k)
FDA Class 2
·Dental
Oniris
FDA 510(k)
FDA Class 2
·Dental
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·November 12, 1999
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·January 7, 1999
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·March 18, 1998
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQE·September 17, 2004
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQE·April 16, 2001
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·June 23, 1999
PHACOEMULSIFICAITON DEVICE
FDA Adverse Event
Malfunction
·*·Product code HQC·February 21, 1997
SERIES TWENTY THOUSAND LEGACY & ACCESSORIES
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·November 1, 1996
INFINITI VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CENTER·Product code HQC·November 12, 2003
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Malfunction
·ALCON LABORATORIES, INC.·Product code HQE·February 27, 1998
UNIVERSAL
FDA Adverse Event
Malfunction
·ALCON - HOUSTON·Product code HQE·February 14, 2003
XTREMEBEAM
FDA Adverse Event
Malfunction
·BFW INC.·Product code FST·September 7, 2010
SERIES TWENTY THOUSAND LEGACY
FDA Adverse Event
Injury
·ALCON-HOUSTON·Product code HQE·May 7, 2004
FLUOROSCOPIC X-RAY
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·August 14, 2007
ACRYSOF IQ NATURAL SINGLEPIECE IOL
FDA Adverse Event
Injury
·ALCON LABORATORIES IRELAND LTD.·Product code HQL·May 6, 2019
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Malfunction
·ALCON-IRVINE TECHNOLOGY CTR·Product code HQC·October 21, 2014