Focused Cryo, Inc.
Country not established
- Devices
- 3
What Focused Cryo, Inc. makes
Focused Cryo, Inc. manufactures a Focused Cryotherapy System, designed for controlled tissue ablation using cryogenic temperatures to treat targeted areas in medical procedures.
The company’s device portfolio is classified under Class II and is listed in the FDA’s 510(k) registry, reflecting its regulatory compliance in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
Focused Cryotherapy System Ref K250742
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 117603202
- [email protected]
- Phone
- 4045944280
Frequently asked questions
How many devices does Focused Cryo, Inc. have in the registry?
The registry currently lists 3 devices for Focused Cryo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Focused Cryo, Inc.'s devices?
Among its 3 most recently registered devices, Focused Cryo, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Focused Cryo, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Focused Cryo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Focused Cryo, Inc. in the registry?
The most recently registered devices listed for Focused Cryo, Inc. include Focused Cryotherapy System Directional Cryoprobe FC-2021CD01, Focused Cryotherapy System Console FC-AR401 and Focused Cryotherapy System.