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App icon of MindMotion Go, from the App Store

Is MindMotion Go FDA approved or cleared?

Yes. MindMotion Go by MindMaze SA is named in the FDA register with a 510(k) clearance, latest decision in 2018.

In the EU: CE class IIa, found in EUDAMED. The manufacturer holds a valid notified body certificate under the MDR in EUDAMED.

At a glance

ProductMindMotion Go
MakerMindMaze SA
Care areaBrain & nerves
What it doesHome-based digital neurotherapeutics for stroke rehabilitation
FDA510(k), latest decision 2018
Verification levelExact product named in the FDA record (checked 18 October 2026)
EU (CE)Class IIa
EU certificateManufacturer certificate from a notified body (MDR) in EUDAMED (checked 18 October 2026)
Websitemindmaze.com
StatusFDA verified
Last checked6 October 2026

Certification status can change. Always confirm in the official register before relying on it: the FDA databases, EUDAMED or the BfArM DiGA directory.

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