Cryon-X LLC
United Statesfrom the FDA registration address FDA establishment FEI 3033648890
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3033648890
- Address
- 1 Parrott Dr Ste 400, Shelton, CT, 06484
Frequently asked questions
How many devices does CRYON-X LLC have in the registry?
The registry currently lists 2 devices for CRYON-X LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list CRYON-X LLC's devices?
Among its 2 most recently registered devices, CRYON-X LLC has devices listed in FDA GUDID (2 devices).
What risk classes do CRYON-X LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for CRYON-X LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CRYON-X LLC in the registry?
The most recently registered devices listed for CRYON-X LLC include Cryon-X Pro CX-152 and Cryon-X One CX-151.