Data / Medical devices / Fentanyl And Other Opioid Protection Glove / Thailand
FDA-registered makers of Fentanyl And Other Opioid Protection Glove in Thailand: 12 establishments
12 establishments in Thailand 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
- Thailand
Makers of Fentanyl And Other Opioid Protection Glove in Thailand
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ansell (thailand) Ltd. | THAILAND Krung Thep Maha Nakhon, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jasmine Glove | Hat Yai Songkhla, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mercator Medical (thailand) Ltd. | Ratthaphum Songkhla, Thailand | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Safeskin Medical & Scientific (thailand), Ltd. | SADAO Songkhla, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sri Trang Gloves (thailand) Public Company Limited. | Hat Yai Songkhla, Thailand | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STGT Anv | Sadao Songkhla, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STGT CP | Pathio Chumphon, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STGT PS1 | Sadao Songkhla, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STGT SR3 | Kanchanadit Surat Thani, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| STGT Surat Thani | Phlai Wat , Kanchanadit Surat Thani, Thailand | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Top Glove Medical (thailand) Co., Ltd. | Sadao District Songkhla, Thailand | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vanda Glove | Pahtong, Hat Yai Songkhla, Thailand | 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.