27 results
·
27ms
·
Sources: EU EUDAMED, US FDA
LUTE; CORE
FDA 510(k)
FDA Class 2
·Dental
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040010426·Zirlux 16+ A4 100X18
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290187·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290132·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290125·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290118·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290088·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290170·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290101·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0115100·Handle, Targeting Needle
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290156·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290095·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290071·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033290149·
ADVANTA SST GRAFT (<6MM)
FDA 510(k)
FDA Class 2
·Cardiovascular
SHIMADZU MOBILE X-RAY SYSTEM MUX-100 SERIES
FDA 510(k)
FDA Class 2
·Radiology
RESTORE
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 29, 2019
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 17, 2021
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code MEB·September 4, 2024
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·May 14, 2018