Data / Medical devices / Cover, Shoe, Operating-Room / Vietnam
FDA-registered makers of Cover, Shoe, Operating-Room in Vietnam: 8 establishments
8 establishments in Vietnam are registered with the FDA to make Cover, Shoe, Operating-Room (product code FXP). 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
- Cover, Shoe, Operating-Room
- Product code
- FXP
- Country
- Vietnam
Makers of Cover, Shoe, Operating-Room in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| An Lanh Investment And Trading Company Limited | Thanh Nam Ward Ninh Binh, Vietnam | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Environstar Group Company Limited | Hung Yen Province, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GLX Medical Devices Company Limited | Bien Hoa Dong Nai, Vietnam | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Liang Cheng Sporting Goods Company Limited | Ben Cat Ward Ho Chi Minh, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MB Regentox Vietnam Trading Service Company Limited | Ho Chi Minh City, Vietnam | Foreign private label distributor, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quang Nam Medical Devices Factory Branch Of Danameco Medical Joint Stock Corporation | Dien Ban Bac Ward Da Nang, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanmu (vietnam) Protective Products Co., Ltd | Duc Hoa Commune Tay Ninh, Vietnam | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sanqi (Vietnam) New Material Co., Ltd | Tan Phuoc 3 Commune Dong Thap, Vietnam | 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.