39 results
·
21ms
·
Sources: EU EUDAMED, US FDA
ORTHOPHOS DS/DC CEPH, ORTHOPHOS 5/PLUS/CD
FDA 510(k)
FDA Class 2
·Dental
8013650
FDA Adverse Event
Malfunction
·October 29, 2018
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027484·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531570·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027507·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027477·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531624·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012856·PedFuse Remind LES, Quad-H, 5.5mm x 50mm
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345026292·Removal Tool
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027422·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027491·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027521·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027460·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531594·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027514·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531587·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531631·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531563·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304027446·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00193033531648·