Data / Medical devices / France / Ricarimpex
Ricarimpex: FDA-registered device maker in EYSINES Nouvelle-Aquitaine, France, 1 510(k) clearance
Ricarimpex is registered with the FDA (registration 3009106257) in EYSINES Nouvelle-Aquitaine, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 21, 2004. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3009106257
- Address
- 245 Avenue De Saint Medard, EYSINES Nouvelle-Aquitaine, France, 33320
- Owner or operator
- RICARIMPEX (10034150)
- Roles
- Manufacturer
- First device listed
- November 10, 2010
- Registered through
- 2027
- Brand names listed
- RICARIMPEX, RICARIMPEX SAS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Leeches, Medicinal | NRN | U | 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 |
|---|---|---|---|---|---|---|
| June 21, 2004 | K040187 | MEDICINAL LEECHES | NRN | Substantially Equivalent | Ricarimpex Sas | accessdata.fda.gov |
Compare with other makers
Updated June 21, 2004. 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.