Data / Medical devices / United States / Aurident, Inc.
Aurident, Inc.: FDA-registered device maker in Fullerton, CA, United States, 1 510(k) clearance
Aurident, Inc. is registered with the FDA (registration 2023817) in Fullerton, CA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2023817
- Address
- 610 South State College BLVD., Fullerton, CA, United States, 92831
- Owner or operator
- AURIDENT, INC. (2023817)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- October 7, 2003
- Registered through
- 2026
- Brand names listed
- Aurident Alloys, Delta Zirconia
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alloy, Gold-Based Noble Metal | EJT | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Alloy, Other Noble Metal | EJS | 2 | Manufacturer | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Repackager or relabeler | 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 17, 2004 | K042638 | RADIANCE PORCELAIN | EIH | Substantially Equivalent | Aurident, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Powder, Porcelain
- All makers of Alloy, Gold-Based Noble Metal
- All makers of Alloy, Other Noble Metal
Updated December 17, 2004. 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.