Data / Medical devices / France / Menicon Pharma SAS
Menicon Pharma SAS: FDA-registered device maker in ILLKIRCH-GRAFFENSTADEN Bas-Rhin, France, 1 510(k) clearance
Menicon Pharma SAS is registered with the FDA (registration 3003779166) in ILLKIRCH-GRAFFENSTADEN Bas-Rhin, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 3, 2013. Registered through 2026. 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
- 3003779166
- Address
- BLD Sebastien Brant Parc D Innovation, ILLKIRCH-GRAFFENSTADEN Bas-Rhin, France, 67400
- Owner or operator
- MENICON CO. LTD. (9001029)
- Roles
- Manufacturer
- First device listed
- July 7, 2013
- Registered through
- 2026
- Brand names listed
- Menicon Unique pH Multi-Purpose Solution
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Products, Contact Lens Care, Rigid Gas Permeable | MRC | 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 |
|---|---|---|---|---|---|---|
| July 3, 2013 | K130805 | MENICON UNIQUE PH MULTI-PURPOSE SOLUTION | MRC | Substantially Equivalent | Menicon Co, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 3, 2013. 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.