Data / Medical devices / France / Damae Medical
Damae Medical: FDA-registered device maker in Paris Ile-de-France, France, 2 510(k) clearances
Damae Medical is registered with the FDA (registration 3027259266) in Paris Ile-de-France, France. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated October 7, 2025. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3027259266
- Address
- 14 rue Sthrau, Paris Ile-de-France, France, 75013
- Owner or operator
- DAMAE MEDICAL (10091159)
- Roles
- Manufacturer
- First device listed
- July 15, 2024
- Registered through
- 2027
- Brand names listed
- deepLive, deepLive DMS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Imaging, Optical Coherence Tomography (Oct) | NQQ | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| October 7, 2025 | K252851 | deepLive (OSP12 + DMS) | NQQ | Substantially Equivalent | Damae Medical | accessdata.fda.gov |
| July 9, 2024 | K240610 | deepLive | NQQ | Substantially Equivalent | Damae Medical | accessdata.fda.gov |
Compare with other makers
Updated October 7, 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.