41 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HARD RELINER
FDA 510(k)
FDA Class 2
·Dental
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252864·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252871·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252796·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252840·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252772·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252833·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252857·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252802·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252819·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252789·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033252826·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112070·Tap, Cannulated, 5.5 mm
AMS FASCIAL-ANCHORING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TRIFLANGE ACETABULAR CUP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AZURION
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·September 11, 2025
TROCAR
FDA Adverse Event
Injury
·MERIT MEDICAL SYSTEMS, INC.·Product code DYB·June 5, 2018
IPC® STYLUS TRANSNASAL BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code ERL·February 6, 2015
IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4
FDA Adverse Event
Malfunction
·MEDTRONIC, INC·Product code ERL·June 19, 2015
XPS® BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·September 8, 2017