Is OMRON Complete & AFib BP monitors FDA approved or cleared?
Yes. OMRON Complete & AFib BP monitors by Omron Healthcare, Inc. is named in the FDA register with a De Novo authorisation, first authorised in 2021, latest decision in 2024.
In the EU: no CE listing found in EUDAMED. Not every CE-marked device is registered there yet.
At a glance
| Product | OMRON Complete & AFib BP monitors |
|---|---|
| Maker | Omron Healthcare, Inc. |
| Care area | Heart & circulation |
| What it does | Home blood pressure monitors with built-in EKG (Complete) and atrial fibrillation screening, synced to OMRON Connect app |
| FDA | De Novo, latest decision 2024 |
| Verification level | Exact product named in the FDA record (checked 18 October 2026) |
| EU (CE) | No CE listing found |
| Website | omronhealthcare.com |
| Status | FDA verified |
| Last checked | 7 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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