Data / Medical devices / Device, Transfer, Patient, Manual / Vietnam
FDA-registered makers of Device, Transfer, Patient, Manual in Vietnam: 8 establishments
8 establishments in Vietnam are registered with the FDA to make Device, Transfer, Patient, Manual (product code FMR). 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
- Device, Transfer, Patient, Manual
- Product code
- FMR
- Country
- Vietnam
Makers of Device, Transfer, Patient, Manual in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 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 | |
| Hengxin (VN) Medical Disposables Co., Ltd. | Trang Bang Tay Ninh, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jiayi Company Limited | DUC HOA COMMUNE Tay Ninh, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| John Snow Vietnam Company Limited | Ho Chi Minh City Binh Duong, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| John Snow Vietnam Company Limited | Ho Chi Minh City, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lotus Packaging Trading Service Production Joint Stock Company. | Ho Chi Minh City, Vietnam | Contract 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.