Actuvi
Country not established FDA establishment FEI 3042366036
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
Company details
- FDA FEI number
- 3042366036
- Address
- 4245 N Central Expy Ste 490, Dallas, TX, 75205
Frequently asked questions
How many devices does ACTUVI have in the registry?
The registry currently lists 1 device for ACTUVI. Devices recorded under merged duplicate company entries are counted once.
Which registries list ACTUVI's devices?
Among its 1 most recently registered device, ACTUVI has devices listed in FDA GUDID (1 device).
What risk classes do ACTUVI's devices fall under?
Among its 1 most recently registered device, the classes recorded for ACTUVI's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from ACTUVI in the registry?
The most recently registered devices listed for ACTUVI include Actuvi 1.0.