Sana Health
United Statesfrom the FDA registration address FDA FEI 3023815184
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Sana Device Ref DEN250005
Regimes: De Novo Registry: De Novo
Company details
- FDA FEI number
- 3023815184
- Address
- 2051 Dogwood St. Ste 110, Louisville, CO, 80027
Frequently asked questions
How many devices does Sana Health have in the registry?
The registry currently lists 2 devices for Sana Health. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sana Health's devices?
Among its 2 most recently registered devices, Sana Health has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Sana Health's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sana Health's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sana Health in the registry?
The most recently registered devices listed for Sana Health include Sana Beta MK4 and Sana Device.