Pharaoh Neuro, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3042638647
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3042638647
- Address
- 1015 Glenwood Ave Fl 4, Minneapolis, MN, 55405
Frequently asked questions
How many devices does PHARAOH NEURO, INC. have in the registry?
The registry currently lists 3 devices for PHARAOH NEURO, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list PHARAOH NEURO, INC.'s devices?
Among its 3 most recently registered devices, PHARAOH NEURO, INC. has devices listed in FDA GUDID (3 devices).
What risk classes do PHARAOH NEURO, INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for PHARAOH NEURO, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from PHARAOH NEURO, INC. in the registry?
The most recently registered devices listed for PHARAOH NEURO, INC. include MindsEye Expandable Port 5.2cm, MindsEye Expandable Port 6.2cm and MindsEye Expandable Port 7.7cm.