Data / Medical devices / Electrosurgical, Cutting & Coagulation & Accessories / Taiwan
FDA-registered makers of Electrosurgical, Cutting & Coagulation & Accessories in Taiwan: 8 establishments
8 establishments in Taiwan are registered with the FDA to make Electrosurgical, Cutting & Coagulation & Accessories (product code GEI). 5 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
- Electrosurgical, Cutting & Coagulation & Accessories
- Product code
- GEI
- Country
- Taiwan
Makers of Electrosurgical, Cutting & Coagulation & Accessories in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| New Deantronics Taiwan Ltd. | New Taipei City, Taiwan | Contract manufacturer, Manufacturer | 11 | October 1, 2025 | 0 | 0 | 0 | api.fda.gov |
| Compal Electronics, Inc | Taoyuan City, Taiwan | Manufacturer | 1 | June 30, 2023 | 0 | 0 | 0 | api.fda.gov |
| Lagis Enterprise Co., Ltd. | Dajia Dist, Taichung City, Taiwan | Manufacturer | 1 | May 20, 2026 | 0 | 0 | 0 | api.fda.gov |
| Unimax Medical Systems Inc. | New Taipei City, Taiwan | Exporter to the US, Specification developer | 1 | December 20, 2011 | 0 | 0 | 0 | api.fda.gov |
| Unimax Medical Systems Inc. | Yilan County, Taiwan | Manufacturer | 1 | December 20, 2011 | 0 | 0 | 0 | api.fda.gov |
| Clearmind Biomedical | Taipei City, Taiwan | Exporter to the US, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| New Deantronics Taiwan Ltd. - Chiayi | Chiayi County Chiayi(County), Taiwan | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| New V-Key Technology Co., Ltd. | New Taipei City, Taipei, Taiwan | Contract 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.