315 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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sensiFirm
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNGO.CT CORONARY ANALYSIS
FDA 510(k)
FDA Class 2
·Radiology
FLUOROPERM 92, 60, 30 AND 151 AND PARAGON HDS, HDS 100 AND THIN RIGID GAS PERMEABLE CONTACT LENSES
FDA 510(k)
FDA Class 2
·Ophthalmic
FATHOM 16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·April 7, 2025
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·December 13, 2024
FATHOM? -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·June 23, 2025
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·December 3, 2024
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·March 19, 2025
FATHOM? -16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·November 6, 2025
FATHOM -16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·October 31, 2024
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·December 6, 2024
CARPENTIER-EDWARDS® CLASSIC ANNULOPLASTY RING
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code KRH·October 14, 2014
ST JUDE ICD
FDA Adverse Event
Injury
·ST JUDE·Product code NIK·July 6, 2011
THERMOPHORE AUTOMATIC MOIST HEAT PACK
FDA Adverse Event
Malfunction
·BATTLE CREEK EQUIPMENT COMPANY·Product code IRT·April 18, 2013
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 11, 2012
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·December 4, 2024
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 11, 2012
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·December 3, 2024
FATHOM -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·December 3, 2024
FATHOM? -16
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code DQX·May 14, 2025