Is Oxitone 1000M FDA approved or cleared?
Yes. Oxitone 1000M by Oxitone Medical Ltd. is named in the FDA register with a 510(k) clearance, latest decision in 2017.
In the EU: no CE listing found in EUDAMED. Not every CE-marked device is registered there yet.
At a glance
| Product | Oxitone 1000M |
|---|---|
| Maker | Oxitone Medical Ltd. |
| Care area | Vital signs & remote monitoring |
| What it does | Continuous pulse oximetry monitoring watch for oxygen saturation tracking |
| FDA | 510(k), latest decision 2017 |
| Verification level | Exact product named in the FDA record (checked 18 October 2026) |
| EU (CE) | No CE listing found |
| Website | oxitone.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