Data / Medical devices / France / Naox Technologies SAS
Naox Technologies SAS: FDA-registered device maker in Paris Ile-de-France, France, 1 510(k) clearance
Naox Technologies SAS is registered with the FDA (registration 3043014934) in Paris Ile-de-France, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 25, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043014934
- Address
- 62 rue mazarine, Paris Ile-de-France, France, 75006
- Owner or operator
- NAOX TECHNOLOGIES (10094901)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- January 5, 2026
- Registered through
- 2026
- Brand names listed
- Naox Link
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Reduced- Montage Standard Electroencephalograph | OMC | 2 | Complaint file establishment, 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 25, 2025 | K251550 | NX01 (NX01) | OMC | Substantially Equivalent | Naox Technologies Sas | accessdata.fda.gov |
Compare with other makers
Updated November 25, 2025. 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.