Data / Medical devices / United States / Movano Inc. Dba Movano Health
Movano Inc. Dba Movano Health: FDA-registered device maker in Pleasanton, CA, United States, 1 510(k) clearance
Movano Inc. Dba Movano Health is registered with the FDA (registration 3027222147) in Pleasanton, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 29, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3027222147
- Address
- 6800 Koll Center Pkwy Ste 160, Pleasanton, CA, United States, 94566
- Owner or operator
- Movano Inc. dba Movano Health (10092114)
- Roles
- Specification developer
- First device listed
- December 5, 2024
- Registered through
- 2026
- Brand names listed
- EvieMED Ring
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Oximeter | DQA | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 29, 2024 | K241090 | Evie Med Ring | DQA | Substantially Equivalent | Movano Inc. Dba Movano Health | accessdata.fda.gov |
Compare with other makers
Updated November 29, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.