Manufacturer registered with FDA
Bernard Cervos Societe (B.C.S) S.A.S
Chassieu, Rhone Alpes, France. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 3
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1France
Devices listed with FDA
What Bernard Cervos Societe (B.C.S) S.A.S currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Porcelain PowderEIH · Class 2 | Dental ceramics & zirconia | Lister | X-Cera Pre-shaded Zirconia BlancksX-Cera Zirconia Blanks | 2025 |
| Base Metal AlloyEJH · Class 2 | Dental alloys | Maker | Alloy, Metal, Base | 2022 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Bernard Cervos Societe (B.C.S) S.A.S lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Dongguan Xiangtong Co., Ltd. (1), Shenzhen Xiangtong Photoelectricity Technology Co., Ltd. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 10 Dec 2020 | K202673 | X-cera Pre-shaded Zirconia Blanks | Dongguan Xiangtong Co., Ltd. | EIH Porcelain Powder |
| 29 Mar 2016 | K153767 | X-cera Zirconia Blanks | Shenzhen Xiangtong Photoelectricity Technology Co., Ltd. | EIH Porcelain Powder |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| BERNARD CERVOS SOCIETE (B.C.S) S.A.SFDA reg. 3024792419 | Chassieu, Rhone Alpes Auvergne-Rhone-Alpes, France | Foreign exporter, Manufacturer, Specification developer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10086092). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.