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Is CognifiSense VRNT FDA approved or cleared?

Yes. CognifiSense VRNT by CognifiSense, Inc. is named in the FDA register with a 510(k) clearance, first authorised in 2023, latest decision in 2026.

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

At a glance

ProductCognifiSense VRNT
MakerCognifiSense, Inc.
Care areaPain & neuromodulation
What it doesVirtual reality therapy for chronic pain
FDA510(k), latest decision 2026
Verification levelExact product named in the FDA record (checked 18 October 2026)
EU (CE)No CE listing found
Websitecognifisense.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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