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Data / Medical devices / System, Measurement, Blood-Pressure, Non-Invasive / Vietnam

FDA-registered makers of System, Measurement, Blood-Pressure, Non-Invasive in Vietnam: 7 establishments

7 establishments in Vietnam are registered with the FDA to make System, Measurement, Blood-Pressure, Non-Invasive (product code DXN). 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
System, Measurement, Blood-Pressure, Non-Invasive
Product code
DXN
Country
Vietnam

Makers of System, Measurement, Blood-Pressure, Non-Invasive in Vietnam

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
ONFU electronics Co., LTD.Trang Bom Dong Nai, VietnamContract manufacturer, Manufacturer7August 6, 2025000api.fda.gov
A&D Vietnam LimitedTu Son Ward Bac Ninh, VietnamManufacturer6May 17, 2017000api.fda.gov
Giantsun Power Electronics (vietnam) Co., LtdHanoi Ha Noi, VietnamContract manufacturer0000api.fda.gov
Health & Life Medical Technology Company LimitedBac Ninh Province, VietnamContract manufacturer0000api.fda.gov
Jamr Technology Company LimitedBen Cat Binh Duong, VietnamContract manufacturer0000api.fda.gov
Omron Healthcare Manufacturing Vietnam Co., Ltd.Ho Chi Minh City, VietnamContract manufacturer0000api.fda.gov
Telstar Vietnam Company LimitedBac Ninh, VietnamContract manufacturer0000api.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.