Corvascular
United Statesfrom the FDA registration address FDA establishment FEI 3033275035
- Devices
- 10
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3033275035
- Address
- 5810 Baker Rd Ste 125, Minnetonka, MN, 55345
Frequently asked questions
How many devices does CORVASCULAR have in the registry?
The registry currently lists 10 devices for CORVASCULAR. Devices recorded under merged duplicate company entries are counted once.
Which registries list CORVASCULAR's devices?
Among its 10 most recently registered devices, CORVASCULAR has devices listed in FDA GUDID (10 devices).
What risk classes do CORVASCULAR's devices fall under?
Among its 10 most recently registered devices, the classes recorded for CORVASCULAR's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CORVASCULAR in the registry?
The most recently registered devices listed for CORVASCULAR include VasoGuard H1V06, VasoGuard H1V08, VasoGuard H1V10 and VasoGuard H2V04.