Data / Medical devices / France / Medecom
Medecom: FDA-registered device maker in PLOUGASTEL DAOULAS Bretagne, France, 1 510(k) clearance
Medecom is registered with the FDA (registration 3010966991) in PLOUGASTEL DAOULAS Bretagne, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 23, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010966991
- Address
- 31 Rue du Pere Gwenael 2nd floor, PLOUGASTEL DAOULAS Bretagne, France, 29470
- Owner or operator
- MEDECOM (10046982)
- Roles
- Manufacturer
- First device listed
- June 9, 2014
- Registered through
- 2026
- Brand names listed
- Med WS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| May 23, 2014 | K132684 | MEDWS SOFTWARE (VARIANTS MEDVIEW, MEDDIAG, MEDMAMMO) | LLZ | Substantially Equivalent | Medecom Sarl | accessdata.fda.gov |
Compare with other makers
Updated May 23, 2014. 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.