Data / Medical devices / China / Qinhuangdao Silide Ceramic Technology Co., Ltd.
Qinhuangdao Silide Ceramic Technology Co., Ltd.: FDA-registered device maker in Qinhuangdao Hebei, China, 1 510(k) clearance
Qinhuangdao Silide Ceramic Technology Co., Ltd. is registered with the FDA (registration 3013136463) in Qinhuangdao Hebei, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 29, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013136463
- Address
- No. 1, Yanghe Road Qinhuangdao Economic and Technologic Development Zone, Qinhuangdao Hebei, China, 066000
- Owner or operator
- Qinhuangdao Silide Ceramic Technology Co., Ltd. (10062311)
- Roles
- Contract manufacturer, Contract sterilizer, Exporter to the US, Foreign private label distributor, Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer
- First device listed
- January 10, 2020
- Registered through
- 2026
- Brand names listed
- Ceramic Denture Zirconia Ceramics Block
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powder, Porcelain | EIH | 2 | Contract manufacturer, Contract sterilizer, Exporter to the US, Foreign private label distributor, Manufacturer, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 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 |
|---|---|---|---|---|---|---|
| November 29, 2018 | K181816 | Ceramic Denture Zirconia Ceramics Block | EIH | Substantially Equivalent | Qinhuangdao Silide Ceramic Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated November 29, 2018. 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.