Data / Medical devices / France / Advanced Medical Solutions (Nantes) SAS
Advanced Medical Solutions (Nantes) SAS: FDA-registered device maker in VIGNEUX DE BRETAGNE Loire-Atlantique, France, 4 510(k) clearances
Advanced Medical Solutions (Nantes) SAS is registered with the FDA (registration 3002673655) in VIGNEUX DE BRETAGNE Loire-Atlantique, France. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 15, 2010. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3002673655
- Address
- ZA Les Quatre Nations - 5, rue Edouard Belin, VIGNEUX DE BRETAGNE Loire-Atlantique, France, 44360
- Owner or operator
- ADVANCED MEDICAL SOLUTIONS GROUP PLC (9031453)
- Roles
- Manufacturer
- First device listed
- November 4, 2024
- Registered through
- 2027
- Brand names listed
- 4BONE BCH, ECLIPSE, ECLIPSE Putty, In'Oss, KAINOS+, MBCP, MBCP+, Orastruct and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bone Grafting Material, Synthetic | LYC | 2 | Manufacturer | accessdata.fda.gov |
| Filler, Bone Void, Calcium Compound | MQV | 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 |
|---|---|---|---|---|---|---|
| March 15, 2010 | K093122 | MBCP+ | LYC | Substantially Equivalent | Biomatlante | accessdata.fda.gov |
| June 2, 2006 | K060732 | MBCP GEL | LYC | Substantially Equivalent | Biomatlante | accessdata.fda.gov |
| January 20, 2006 | K051774 | MBCP | MQV | Substantially Equivalent | Biomatlante | accessdata.fda.gov |
| September 16, 2005 | K051885 | MBCP | LYC | Substantially Equivalent | Biomatlante | accessdata.fda.gov |
Compare with other makers
Updated March 15, 2010. 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.