Spiro Robotics Inc.
Also registered as Spiro Robotics
United Statesfrom the FDA registration address FDA establishment FEI 3043712029
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Spiro-VISTA Ref K253437
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043712029
- Address
- 22320 Foothill Blvd Ste 250, Hayward, CA, 94541
Frequently asked questions
How many devices does Spiro Robotics Inc. have in the registry?
The registry currently lists 1 device for Spiro Robotics Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spiro Robotics Inc.'s devices?
Among its 1 most recently registered device, Spiro Robotics Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Spiro Robotics Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Spiro Robotics Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spiro Robotics Inc. in the registry?
The most recently registered devices listed for Spiro Robotics Inc. include Spiro-VISTA.