191 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIAMONDBACK 360 PERIPHERAL ORBITAL ATHERECTOMY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
AGXO
FDA UDI
Oticon A/S·05707131261168·H100, MINIRITE 312 WL SIL AGXO
GENERAL DENISTRY MOTOR
FDA 510(k)
FDA Class 1
·Dental
GEODESIC EEG SYSTEM SERIES 100
FDA 510(k)
FDA Class 2
·Neurology
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 18, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 18, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 20, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·April 21, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 20, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·May 28, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 28, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 15, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 11, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 14, 2026
NEXIVA
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·April 21, 2026
IMP, TSV, 4.7,11,MTX,MC,MG,HA
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·April 3, 2025
IMP, TSV, 4.7,10,MTX,MC,MG,HA
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·August 9, 2022
IMP, TSV, 4.7, 8,MTX,MC,MG,HA
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·May 9, 2023
IMP, TSV, 4.7, 8, MTXF, MG, HA
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·May 27, 2026
IMP, TSV, 4.7, 8, MTXF, MG, HA
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·May 27, 2026