Neurovena Corp.
Country not established
- Devices
- 1
What Neurovena Corp. makes
Neurovena Corp. manufactures the AURORA, a neurostimulation device designed for targeted nerve modulation, primarily used in pain management and functional restoration therapies.
The AURORA is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Aurora Ref K972065
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurovena Corp. have in the registry?
The registry currently lists 1 device for Neurovena Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurovena Corp.'s devices?
Among its 1 most recently registered device, Neurovena Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Neurovena Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurovena Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurovena Corp. in the registry?
The most recently registered devices listed for Neurovena Corp. include AURORA.