Data / Medical devices / Alloy, Other Noble Metal / United States
FDA-registered makers of Alloy, Other Noble Metal in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Alloy, Other Noble Metal (product code EJS). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Alloy, Other Noble Metal
- Product code
- EJS
- Country
- United States
Makers of Alloy, Other Noble Metal in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Sterngold Dental LLC | Attleboro, MA, United States | Manufacturer | 5 | September 19, 2002 | 0 | 0 | 0 | api.fda.gov |
| Aalba Dent, Inc. | Fairfield, CA, United States | Manufacturer | 1 | September 5, 1997 | 0 | 0 | 0 | api.fda.gov |
| Aurident, Inc. | Fullerton, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ivoclar Vivadent, Inc. | Amherst, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jensen Industries, Inc. | North Haven, CT, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Strategy Milling, LLC | Leetsdale, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum Orthodontics Corporation | Monrovia, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Argen Corporation | San Diego, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Argen Corporation | San Diego, CA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| World Lab U.S.A. | Irvine, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.