Neuroinvent, Inc.
Country not established
- Devices
- 2
What Neuroinvent, Inc. makes
Neuroinvent, Inc. manufactures subdermal needle electrodes designed for multi-paired use, intended for medical applications requiring precise electrical signal transmission beneath the skin.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuroinvent, Inc. have in the registry?
The registry currently lists 2 devices for Neuroinvent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuroinvent, Inc.'s devices?
Among its 2 most recently registered devices, Neuroinvent, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Neuroinvent, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Neuroinvent, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuroinvent, Inc. in the registry?
The most recently registered devices listed for Neuroinvent, Inc. include E-Shield Multi-paried Subdermal Needle Electrodes and E-SHIELD MULTI-PAIRED SUBDERMAL NEEDLE ELECTRODES.