Data / Medical devices / Fentanyl And Other Opioid Protection Glove / Vietnam
FDA-registered makers of Fentanyl And Other Opioid Protection Glove in Vietnam: 10 establishments
10 establishments in Vietnam are registered with the FDA to make Fentanyl And Other Opioid Protection Glove (product code QDO). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Fentanyl And Other Opioid Protection Glove
- Product code
- QDO
- Country
- Vietnam
Makers of Fentanyl And Other Opioid Protection Glove in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Basic International Viet Nam Co.,ltd | QUANG TRUNG WARD Thanh Hoa, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ever Global (vietnam) Enterprise Corporation | Dong Nai Province, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ever Global (vietnam) Enterprise Corporation | Long Khanh City Dong Nai, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ever Global (vietnam) Enterprise Corporation | An Phuoc Village Dong Nai, Vietnam | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kanglongda Vietnam Protection Technology Company Limited | Phong Dien Thua Thien-Hue, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| S&S Glove Corporation | Ho Chi Minh City, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| S&S Glove Corporation- Branch 1 | Ho Chi Minh City Ba Ria-Vung Tau, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thanh Hoa Medical Technology Co., Ltd. | QUANG TRUNG WARD Thanh Hoa, Vietnam | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vietmedical Product Co., Ltd. | QUANG TRUNG WARD Thanh Hoa, Vietnam | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vietwell Technology Vietnam Co., Ltd. | Bim Son Thanh Hoa, Vietnam | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.