Data / Medical devices / Alloy, Metal, Base / United States
FDA-registered makers of Alloy, Metal, Base in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Alloy, Metal, Base (product code EJH). 5 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, Metal, Base
- Product code
- EJH
- Country
- United States
Makers of Alloy, Metal, Base in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aalba Dent, Inc. | Fairfield, CA, United States | Manufacturer | 13 | March 4, 2004 | 0 | 0 | 0 | api.fda.gov |
| The Belport Company, Inc DBA Gingi-Pak | Camarillo, CA, United States | Manufacturer | 4 | February 15, 2001 | 0 | 0 | 0 | api.fda.gov |
| Talladium, Inc. | Santa Clarita, CA, United States | Manufacturer | 1 | December 20, 1989 | 0 | 0 | 0 | api.fda.gov |
| The Argen Corporation | San Diego, CA, United States | Manufacturer, Repackager or relabeler | 1 | September 26, 2000 | 0 | 0 | 0 | api.fda.gov |
| The Argen Corporation | San Diego, CA, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 1 | September 26, 2000 | 0 | 0 | 0 | api.fda.gov |
| GC America Inc. | Alsip, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ivoclar Vivadent, Inc. | Amherst, NY, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neodontics Inc | Glendale, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Straumann Manufacturing, Inc. | Mansfield, TX, United States | Contract 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.