Darmiyan, Inc.
United Statesfrom the FDA registration address FDA FEI 3030624673
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
BrainSee Ref DEN220066
Regimes: De Novo Registry: 510(k)
Company details
- FDA FEI number
- 3030624673
- Address
- 900 E Hamilton Ave, Suite 100, Campbell, CA, 95008
Frequently asked questions
How many devices does Darmiyan, Inc. have in the registry?
The registry currently lists 1 device for Darmiyan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Darmiyan, Inc.'s devices?
Among its 1 most recently registered device, Darmiyan, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Darmiyan, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Darmiyan, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Darmiyan, Inc. in the registry?
The most recently registered devices listed for Darmiyan, Inc. include BrainSee.