Skip to the page

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

Alloy, Gold-Based Noble Metal (EJT): 27 FDA-registered makers in 9 countries

27 establishments in 9 countries are registered with the FDA to make Alloy, Gold-Based Noble Metal (product code EJT, Class 2, 21 CFR 872.3060). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 627 510(k) clearances under this code, the latest on October 14, 2005, and lists 0 recall events (0 Class I). 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.

Product code
EJT
Device class
2
Regulation
872.3060
Medical specialty
Dental

Makers by country

CountryMakers
China11
United States8
Germany2
Switzerland1
Hong Kong1
Philippines1
Canada1
South Korea1
Taiwan1

Makers of Alloy, Gold-Based Noble Metal

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

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
Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KGBremen, GermanyManufacturer0000api.fda.gov
Cendres+metaux SABiel/Bienne Bern, SwitzerlandManufacturer0000api.fda.gov
Crown Trading (HK) Co., LimitedHong Kong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Degudent GMBHHANAU Hesse, GermanyManufacturer0000api.fda.gov
Digital Dental Depotzhuhai Guangdong, ChinaContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Digital Dental Depot LimitedHong Kong, Hong KongContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Forbes Dental Prosthetics Inc.Palanan Makati Central Luzon, PhilippinesContract manufacturer0000api.fda.gov
Fseven Dental Technology Zhuhai Co.,ltdZHUHAI Guangdong, ChinaExporter to the US, 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
Ocean CeramicsAldergrove British Columbia, CanadaManufacturer0000api.fda.gov
One Day Dental PartnerSuncheon-si Jeonnam, South KoreaExporter to the US, Manufacturer0000api.fda.gov
Qinhuangdao Audental Metal Technology Co., Ltd.Qinhuangdao City Hebei, ChinaManufacturer0000api.fda.gov
Shen Fu Arts LabShen Zhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen HLD Dental&technology Co.,ltdShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Shenzhen Times Dental LabShenzhen Guangdong, ChinaManufacturer0000api.fda.gov
Smart Dental Cad Solutions LimitedZhuhai Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Smilden Biotechnology Co., Ltd.New Taipei City, TaiwanManufacturer0000api.fda.gov
Strategy Milling, LLCLeetsdale, PA, United StatesManufacturer0000api.fda.gov
Shenzhen Jiahong Dental Technology Co., LtdShenzhen Guangdong, ChinaContract manufacturer0000api.fda.gov
Shenzhen Sunmc Dental Technology Co., Ltd.Shenzhen Guangdong, ChinaManufacturer0000api.fda.gov
The Argen CorporationSan Diego, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Vivi Dental LaboratoryShenzhen Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
World Lab U.S.A.Irvine, CA, United StatesManufacturer for export0000api.fda.gov

Updated October 14, 2005. 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.