Neuvotion, Inc.
United Statesfrom the FDA registration address FDA FEI 3046040683
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Neuvotion, Inc. makes
Neuvotion, Inc. manufactures the NeuStim NN-01, a neuromodulation device designed for targeted nerve stimulation therapy.
The NeuStim NN-01 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Neuvotion NeuStim NN-01 Ref K240632
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046040683
- Address
- 165 Club Rd, Stamford, CT, 06905
Frequently asked questions
How many devices does Neuvotion, Inc. have in the registry?
The registry currently lists 1 device for Neuvotion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuvotion, Inc.'s devices?
Among its 1 most recently registered device, Neuvotion, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuvotion, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuvotion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuvotion, Inc. in the registry?
The most recently registered devices listed for Neuvotion, Inc. include Neuvotion NeuStim NN-01.