Data / Medical devices / China / Fuzhou Rick Brown Biomaterials Co. Ltd.
Fuzhou Rick Brown Biomaterials Co. Ltd.: FDA-registered device maker in Fuzhou Fujian, China, 1 510(k) clearance
Fuzhou Rick Brown Biomaterials Co. Ltd. is registered with the FDA (registration 3029968429) in Fuzhou Fujian, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 3, 2023. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3029968429
- Address
- The first and second floors of R&D Building, Jiecheng Industrial Park, No.36 Houshan Zhaishan, Nanyu Town High-Tech District, Fuzhou, Fujian Province, Fuzhou Fujian, China, 350100
- Owner or operator
- Fuzhou Rick Brown Biomaterials Co. Ltd. (10088829)
- Roles
- Manufacturer
- First device listed
- October 15, 2023
- Registered through
- 2027
- Brand names listed
- Dental Lithium Disilicate Glass-Ceramic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adhesive, Denture, Carboxymethylcellulose Sodium (49%) And Ethylene-Oxide Homopolymer | KXW | 1 | Manufacturer | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Manufacturer | accessdata.fda.gov |
| Restoration, Porcelain | NSP | N | 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, 2023 | K230487 | Dental Lithium Disilicate Glass-Ceramic | EIH | Substantially Equivalent | Fuzhou Rick Brown Biomaterials Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 3, 2023. 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.