Skip to the page

Data / Medical devices / Support, Arm / Vietnam

FDA-registered makers of Support, Arm in Vietnam: 10 establishments

10 establishments in Vietnam are registered with the FDA to make Support, Arm (product code IOY). 0 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
Support, Arm
Product code
IOY
Country
Vietnam

Makers of Support, Arm in Vietnam

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Acode Sporting Goods Company LimitedHo Chi Minh, VietnamExporter to the US, Manufacturer0000api.fda.gov
Actlife Technology Co., Ltd - Thanh Hoa BranchTrung Chinh Commune Thanh Hoa, VietnamManufacturer0000api.fda.gov
Foundation Wellness International Co., LTD (FWIL)Binh Duong, VietnamManufacturer0000api.fda.gov
Global Cases (vietnam) Corporation LimitedTAN UYEN TOWN Binh Duong, VietnamManufacturer0000api.fda.gov
Good Time Health Care Products Co., Ltd.Ho Chi Minh City Binh Duong, VietnamContract manufacturer, Exporter to the US, Manufacturer0000api.fda.gov
Liang Cheng Sporting Goods Company LimitedBen Cat Ward Ho Chi Minh, VietnamContract manufacturer, Manufacturer0000api.fda.gov
Myhung Garment And Trading Joint Stock CompanyMy Hao Dist Hung Yen, VietnamContract manufacturer0000api.fda.gov
Praegear Viet Nam Co., Ltd.Duc Hoa District Long An, VietnamContract manufacturer0000api.fda.gov
Reak Vietnam Company LimitedNhon Trach Commune Dong Nai, VietnamExporter to the US, Manufacturer0000api.fda.gov
Vietnam Yetitech Equipment Company LimitedN/A Hung Yen, VietnamExporter to the US, 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.