Skip to the page

Data / Medical devices / Alloy, Gold-Based Noble Metal / United States

FDA-registered makers of Alloy, Gold-Based Noble Metal in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Alloy, Gold-Based Noble Metal (product code EJT). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Alloy, Gold-Based Noble Metal
Product code
EJT
Country
United States

Makers of Alloy, Gold-Based Noble Metal in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Sterngold Dental LLCAttleboro, MA, United StatesManufacturer7June 26, 2002000api.fda.gov
Aalba Dent, Inc.Fairfield, CA, United StatesManufacturer2August 15, 1997000api.fda.gov
Aurident, Inc.Fullerton, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Ivoclar Vivadent, Inc.Amherst, NY, United StatesManufacturer0000api.fda.gov
Jensen Industries, Inc.North Haven, CT, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Strategy Milling, LLCLeetsdale, PA, United StatesManufacturer0000api.fda.gov
The Argen CorporationSan Diego, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
World Lab U.S.A.Irvine, CA, United StatesManufacturer for export0000api.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.