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Data / Medical devices / Restoration, Porcelain-Fused-To-Metal / Vietnam

FDA-registered makers of Restoration, Porcelain-Fused-To-Metal in Vietnam: 7 establishments

7 establishments in Vietnam are registered with the FDA to make Restoration, Porcelain-Fused-To-Metal (product code NSO). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 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
Restoration, Porcelain-Fused-To-Metal
Product code
NSO
Country
Vietnam

Makers of Restoration, Porcelain-Fused-To-Metal in Vietnam

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aceso Dental Laboratory Company LimitedAn Phuoc Ward Dong Nai, VietnamManufacturer0000api.fda.gov
Dai Thang General Business LtdHo Chi Minh City,, VietnamExporter to the US, Manufacturer0000api.fda.gov
Digital Age Dental Laboratories, Ltd.Vinh Tan Ward Ho Chi Minh, VietnamExporter to the US, Manufacturer0000api.fda.gov
Eastern Dragon TSPHo Chi Minh, VietnamExporter to the US, Manufacturer0000api.fda.gov
Ho Chi Minh Branch - Vatech Viet Joint Stock CompanyThanh My Tay Ward Ho Chi Minh, VietnamManufacturer0000api.fda.gov
Next Lab Joint Stock CompanyTan Phu Ward Ho Chi Minh, VietnamManufacturer, Remanufacturer0000api.fda.gov
Vu Gia Dental Lab Co., Ltd.Hanoi Ha Noi, VietnamContract manufacturer, Manufacturer, Remanufacturer0000api.fda.gov

Updated November 3, 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.