Interfocus Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3043515178
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3043515178
- Address
- 650 CASTRO STREET, STE 120-458, Mountain View, CA, 94041
Frequently asked questions
How many devices does INTERFOCUS INC. have in the registry?
The registry currently lists 1 device for INTERFOCUS INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list INTERFOCUS INC.'s devices?
Among its 1 most recently registered device, INTERFOCUS INC. has devices listed in FDA GUDID (1 device).
What risk classes do INTERFOCUS INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for INTERFOCUS INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from INTERFOCUS INC. in the registry?
The most recently registered devices listed for INTERFOCUS INC. include Mamapro H03.