Inovx, Inc.
Country not established
- Devices
- 1
What Inovx, Inc. makes
Inovx, Inc. manufactures neuroprobes, which are invasive medical devices designed for precise neural recording and stimulation in research and clinical applications.
The company’s neuroprobes fall under FDA Class II regulation and are listed via the 510(k) pathway. The devices are based in the United States.
Catalogue
Neuroprobe Ref K874018
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inovx, Inc. have in the registry?
The registry currently lists 1 device for Inovx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inovx, Inc.'s devices?
Among its 1 most recently registered device, Inovx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Inovx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Inovx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inovx, Inc. in the registry?
The most recently registered devices listed for Inovx, Inc. include NEUROPROBE.