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App icon of GoSpiro, from the App Store

Is GoSpiro FDA approved or cleared?

Yes. GoSpiro by Monitored Therapeutics, Inc. is named in the FDA register with a 510(k) clearance, latest decision in 2020.

In the EU: no CE listing found in EUDAMED. Not every CE-marked device is registered there yet.

At a glance

ProductGoSpiro
MakerMonitored Therapeutics, Inc.
Care areaSleep & breathing
What it doesSmartphone spirometer for lung function testing and respiratory health monitoring
FDA510(k), latest decision 2020
Verification levelExact product named in the FDA record (checked 18 October 2026)
EU (CE)No CE listing found
Websitevitalograph.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.

Need the evidence behind this entry?
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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