Data / Medical devices / Vinyl Patient Examination Glove / Vietnam
FDA-registered makers of Vinyl Patient Examination Glove in Vietnam: 5 establishments
5 establishments in Vietnam are registered with the FDA to make Vinyl Patient Examination Glove (product code LYZ). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Vinyl Patient Examination Glove
- Product code
- LYZ
- Country
- Vietnam
Makers of Vinyl Patient Examination Glove in Vietnam
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ever Global (vietnam) Enterprise Corporation | An Phuoc Village Dong Nai, Vietnam | Contract manufacturer, Manufacturer | 2 | February 6, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ever Global (vietnam) Enterprise Corporation | Dong Nai Province, Vietnam | Contract manufacturer, Manufacturer | 1 | October 19, 2022 | 0 | 0 | 0 | api.fda.gov |
| Ever Global (vietnam) Enterprise Corporation | Long Khanh City Dong Nai, Vietnam | Manufacturer | 1 | December 29, 2017 | 0 | 0 | 0 | api.fda.gov |
| Viet Phu Trade And Import Export Co., Ltd | DONG TRIEU Quang Ninh, Vietnam | Manufacturer | 1 | October 27, 2025 | 0 | 0 | 0 | api.fda.gov |
| Star Investment And Trade Joint Stock Company | Bac Ninh, Vietnam | Exporter to the US, 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.