Is SimpleSense FDA approved or cleared?
Yes. SimpleSense by Nanowear, Inc. is named in the FDA register with a 510(k) clearance, first authorised in 2020, latest decision in 2023.
In the EU: no CE listing found in EUDAMED. Not every CE-marked device is registered there yet.
At a glance
| Product | SimpleSense |
|---|---|
| Maker | Nanowear, Inc. |
| Care area | Heart & circulation |
| What it does | SimpleSense™ is an FDA cleared remote diagnostic platform. The non-invasive undergarment monitors multiple patient vitals such as heart rate and sounds, respiration rate, lung volume, and physical activity. |
| FDA | 510(k), latest decision 2023 |
| Verification level | Exact product named in the FDA record (checked 18 October 2026) |
| EU (CE) | No CE listing found |
| Website | nanowearinc.com |
| Status | FDA verified |
| Last checked | 6 October 2026 |
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
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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