Data / Medical devices / Aid, Transfer / Vietnam
FDA-registered makers of Aid, Transfer in Vietnam: 9 establishments
9 establishments in Vietnam are registered with the FDA to make Aid, Transfer (product code IKX). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Aid, Transfer
- Product code
- IKX
- Country
- Vietnam
Makers of Aid, Transfer in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Evolution Technologies Vietnam. Co. Ltd | Tan Uyen Binh Duong, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fullerton Manufacturing Limited | Da Nang Bac Lieu, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Guangmei VN Production Service Trade Company Limited | Thuan An Binh Duong, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hameco Hy Co., Ltd | Hung Yen Province, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nova Orthopedic And Rehabitation Appliance(vn) Co., Ltd | Ben Cat Ward Ho Chi Minh, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tswen Hoei Enterprise Vietnam Co., Ltd. | Ho Chi Minh City, Vietnam | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viet - Long An Medical Supply Company Ltd. | Long An, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yong Yi Viet Nam Co.,ltd | Duc Hoa Commune Tay Ninh, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zhouyang Medical Vietnam Co., Ltd | Hai Phong, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.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.