Fiagon Na LLC
Country not established FDA FEI 3025490805
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
Company details
- FDA FEI number
- 3025490805
- DUNS number
- 145001318
- Address
- 5000 Township Pkwy, Saint Paul, MN, 55110
Frequently asked questions
How many devices does FIAGON NA LLC have in the registry?
The registry currently lists 6 devices for FIAGON NA LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list FIAGON NA LLC's devices?
Among its 6 most recently registered devices, FIAGON NA LLC has devices listed in FDA GUDID (6 devices).
What risk classes do FIAGON NA LLC's devices fall under?
Among its 6 most recently registered devices, the classes recorded for FIAGON NA LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from FIAGON NA LLC in the registry?
The most recently registered devices listed for FIAGON NA LLC include VenSure™ Balloon Dilation System Non-Navigated, VenSure™ Balloon Dilation System Navigated, VenSure™ Balloon Dilation System 4D and VenSure™ Balloon Dilation System Eustachian Tube.