Data / Medical devices / France / Bernard Cervos Societe (B.C.S) S.A.S
Bernard Cervos Societe (B.C.S) S.A.S: FDA-registered device maker in Chassieu, Rhone Alpes Auvergne-Rhone-Alpes, France, 2 510(k) clearances
Bernard Cervos Societe (B.C.S) S.A.S is registered with the FDA (registration 3024792419) in Chassieu, Rhone Alpes Auvergne-Rhone-Alpes, France. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 10, 2020. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3024792419
- Address
- 17 Rue des freres Lumiere, Chassieu, Rhone Alpes Auvergne-Rhone-Alpes, France, 69680
- Owner or operator
- Bernard Cervos Societe (B.C.S) S.A.S (10086092)
- Roles
- Exporter to the US, Manufacturer, Specification developer
- First device listed
- October 14, 2022
- Registered through
- 2026
- Brand names listed
- Alloy, Metal, Base, X-Cera Pre-shaded Zirconia Blancks, X-Cera Zirconia Blanks
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alloy, Metal, Base | EJH | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| December 10, 2020 | K202673 | X-cera Pre-shaded Zirconia Blanks | EIH | Substantially Equivalent | Dongguan Xiangtong Co., Ltd. | accessdata.fda.gov |
| March 29, 2016 | K153767 | X-cera Zirconia Blanks | EIH | Substantially Equivalent | Shenzhen Xiangtong Photoelectricity Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 10, 2020. 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.