Data / Medical devices / Pad, Menstrual, Reusable / Vietnam
FDA-registered makers of Pad, Menstrual, Reusable in Vietnam: 5 establishments
5 establishments in Vietnam are registered with the FDA to make Pad, Menstrual, Reusable (product code NUQ). 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
- Pad, Menstrual, Reusable
- Product code
- NUQ
- Country
- Vietnam
Makers of Pad, Menstrual, Reusable in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cerie (vietnam) International Limited | BINH NGUYEN COMMUNE Phu Tho, Vietnam | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Crystal Martin (vietnam) Company Limited | Nenh Ward Bac Ninh, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hung Yen South | Hung Yen, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Regina Miracle International (viet Nam) Co., Ltd | Haiphong Hai Phong, Vietnam | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tenfy Technology (vietnam)company Limited | Ben Cau Commune Tay Ninh, Vietnam | Contract manufacturer, Exporter to the US, Manufacturer, Repackager or relabeler | 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.