Data / Medical devices / China / Shen Fu Arts Lab
Shen Fu Arts Lab: FDA-registered device maker in Shen Zhen Guangdong, China, 1 510(k) clearance
Shen Fu Arts Lab is registered with the FDA (registration 3004578725) in Shen Zhen Guangdong, China. It lists 15 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 12, 1980. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004578725
- Address
- 1F,12 Building, Xinxin tian Industrial Park, Xin Sha Road Shajing Town, Shen Zhen Guangdong, China, 518104
- Owner or operator
- SHEN FU ARTS LAB (9063832)
- Roles
- Manufacturer
- First device listed
- September 14, 2004
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alloy, Gold-Based Noble Metal | EJT | 2 | Manufacturer | accessdata.fda.gov |
| Alloy, Metal, Base | EJH | 2 | Manufacturer | accessdata.fda.gov |
| Alloy, Other Noble Metal | EJS | 2 | Manufacturer | accessdata.fda.gov |
| Dentures, Full | NSL | N | Manufacturer | accessdata.fda.gov |
| Dentures, Partial | NSK | N | Manufacturer | accessdata.fda.gov |
| Prosthesis, Orthodontic | NSR | N | Manufacturer | accessdata.fda.gov |
| Resin, Denture, Relining, Repairing, Rebasing | EBI | 2 | Manufacturer | accessdata.fda.gov |
| Restoration, Base Metal | NSQ | N | Manufacturer | accessdata.fda.gov |
| Restoration, Noble Metal | NSJ | N | Manufacturer | accessdata.fda.gov |
| Restoration, Porcelain | NSP | N | Manufacturer | accessdata.fda.gov |
| Restoration, Porcelain-Fused-To-Metal | NSO | N | Manufacturer | accessdata.fda.gov |
| Restoration, Resin | NSM | N | Manufacturer | accessdata.fda.gov |
| Restoration, Resin, Crown And Bridge | NSN | N | Manufacturer | accessdata.fda.gov |
| System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations | NOF | 2 | Manufacturer | accessdata.fda.gov |
| Wax, Dental, Intraoral | EGD | 1 | 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 12, 1980 | K800400 | MAXUM DENTURE RESIN | EBI | Substantially Equivalent | Dentsply Intl. | accessdata.fda.gov |
Compare with other makers
- All makers of Dentures, Partial
- All makers of Alloy, Gold-Based Noble Metal
- All makers of Restoration, Resin
- All makers of Dentures, Full
- All makers of Resin, Denture, Relining, Repairing, Rebasing
- All makers of Alloy, Metal, Base
Updated March 12, 1980. 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.