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Data / Medical devices / Alloy, Other Noble Metal

Alloy, Other Noble Metal (EJS): 30 FDA-registered makers in 9 countries

30 establishments in 9 countries are registered with the FDA to make Alloy, Other Noble Metal (product code EJS, 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 194 510(k) clearances under this code, the latest on August 19, 2004, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
EJS
Device class
2
Regulation
872.3060
Medical specialty
Dental

Makers by country

CountryMakers
China12
United States10
Germany2
Switzerland1
Hong Kong1
Philippines1
Italy1
South Korea1
United Kingdom1

Makers of Alloy, Other 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 StatesManufacturer5September 19, 2002000api.fda.gov
Aalba Dent, Inc.Fairfield, CA, United StatesManufacturer1September 5, 1997000api.fda.gov
Aidite (qinhuangdao) Technology Co., LtdQinhuangdao City Hebei, ChinaManufacturer0000api.fda.gov
Aurident, Inc.Fullerton, CA, United StatesManufacturer0000api.fda.gov
Bego Bremer Goldschlaegerei Wilh. Herbst GMBH & Co. KGBremen, GermanyManufacturer0000api.fda.gov
Cendres+metaux SABiel/Bienne Bern, SwitzerlandManufacturer0000api.fda.gov
Deprag High Tech Materials ( Zhengzhou ) Co.,ltd.ZHANGZHOU Henan, ChinaManufacturer0000api.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
Dentaurum GmbH & Co. KGISPRINGEN Baden-Wurttemberg, GermanyManufacturer0000api.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
Hunan Ceramaster Material Technology Co., LtdChangsha Hunan, ChinaManufacturer0000api.fda.gov
Ivoclar Vivadent, Inc.Amherst, NY, United StatesManufacturer0000api.fda.gov
Jensen Industries, Inc.North Haven, CT, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Leone SPASesto Fiorentino Firenze, ItalyManufacturer, Specification developer0000api.fda.gov
Liaoning Xinaite Technology Co.,ltdbenxi Liaoning, ChinaManufacturer0000api.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
Strategy Milling, LLCLeetsdale, PA, United StatesManufacturer0000api.fda.gov
Sunrise Dental Laboratory, Ltd.Kowloon, Hong Kong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Shandong Huge Dental Material CorporationRizhao Shandong, ChinaManufacturer0000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
The Argen CorporationSan Diego, CA, United StatesManufacturer, Repackager or relabeler0000api.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
Wright Health GroupDundee Dundee City, United KingdomSpecification developer0000api.fda.gov

Updated August 19, 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.