Data / Medical devices / Gauze / Sponge,Nonresorbable For External Use / Taiwan
FDA-registered makers of Gauze / Sponge,Nonresorbable For External Use in Taiwan: 8 establishments
8 establishments in Taiwan are registered with the FDA to make Gauze / Sponge,Nonresorbable For External Use (product code NAB). 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
- Gauze / Sponge,Nonresorbable For External Use
- Product code
- NAB
- Country
- Taiwan
Makers of Gauze / Sponge,Nonresorbable For External Use in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anti-Microbial Savior Bioteq Co., Ltd. | Kaohsiung City, Taiwan | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| China Surgical Dressings Center Co.,ltd | CHANGHWA CITY, FU-TIEN LI Changhua, Taiwan | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Green Energy Nano Technology Co., Ltd | New Taipei City, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Modern Healthcare Corp. | TIEN CHUNG COUNTY, CHANG-HWA Changhua, Taiwan | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oriental Resources Development Limited | Hukou Township Hsinchu(County), Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sundex Corporation | Taipei, Taiwan | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tronjen Medical Technology Inc | Nantun Dist. Taichung, Taiwan | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Yasco Enterprise Corp. | Chiayi County Chiayi(County), Taiwan | 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.