Data / Medical devices / Container, Specimen, Non-Sterile / Vietnam
FDA-registered makers of Container, Specimen, Non-Sterile in Vietnam: 9 establishments
9 establishments in Vietnam are registered with the FDA to make Container, Specimen, Non-Sterile (product code NNI). 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
- Container, Specimen, Non-Sterile
- Product code
- NNI
- Country
- Vietnam
Makers of Container, Specimen, Non-Sterile in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Grand Aurora Company Limited | Binh Duong Province, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| M.D. Japan, Ltd | Can Giuoc District Long An, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Meditec Technology Company Limited | Bac Ninh, Vietnam | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mida Precision Mold Co.,ltd | BEN LUC DISTRICT Long An, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mida Precision Mold Corporation | My Yen Commune Tay Ninh, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ningbo Changya Plastic (vietnam) Co., Ltd. | Tay Ninh Province, Vietnam | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ta Ting Plastic (hai Duong) Co.,ltd | Cam Giang Commune Hai Phong, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vburg Infant Products Co.,ltd | TuKy District Hai Duong, Vietnam | Complaint file establishment, Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| VS Industry Vietnam Joint Stock Company | Bac Ninh City, 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.