OpenMotion AI, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3017723982
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3017723982
- Address
- 15431 Fitzhugh Rd Ste 208, Dripping Springs, TX, 78620
Frequently asked questions
How many devices does OpenMotion AI, Inc. have in the registry?
The registry currently lists 2 devices for OpenMotion AI, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list OpenMotion AI, Inc.'s devices?
Among its 2 most recently registered devices, OpenMotion AI, Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do OpenMotion AI, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for OpenMotion AI, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from OpenMotion AI, Inc. in the registry?
The most recently registered devices listed for OpenMotion AI, Inc. include MotionSleeve MS-U-01 and MotionSleeve MS-L-01.