Is Neuronaute EEG system FDA approved or cleared?
Yes. Neuronaute EEG system by BioSerenity SAS is named in the FDA register with a 510(k) clearance, first authorised in 2017, latest decision in 2023.
In the EU: CE class IIa, found in EUDAMED. No notified body certificate is visible in EUDAMED yet; ask the maker for it (devices still under the older MDD rules often have none listed).
At a glance
| Product | Neuronaute EEG system |
|---|---|
| Maker | BioSerenity SAS |
| Care area | Brain & nerves |
| What it does | Portable EEG monitoring system for neurological assessment |
| FDA | 510(k), latest decision 2023 |
| Verification level | Exact product named in the FDA record (checked 18 October 2026) |
| EU (CE) | Class IIa |
| EU certificate | Not visible in EUDAMED yet (checked 18 October 2026) |
| Website | bioserenity.com/neuronaute |
| Status | FDA verified |
| Last checked | 6 October 2026 |
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Certified Health Apps Pro gives you the FDA reference number, decision date and a direct link to the official record, plus the EU certificate and notified body, for every app. See Pro · Free guide: how to check a health app in two minutes
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