Data / Medical devices / Taiwan / Coforce Medical Co., Ltd.
Coforce Medical Co., Ltd.: FDA-registered device maker in New Taipei City, Taiwan, 1 510(k) clearance
Coforce Medical Co., Ltd. is registered with the FDA (registration 3013273508) in New Taipei City, Taiwan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 26, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013273508
- Address
- 9F.-7 and 9F.-8 No. 97, Sec. 1, Xintai 5th Road Xizhi District, New Taipei City, Taiwan, 221
- Owner or operator
- Coforce Medical Co., Ltd. (10093646)
- Roles
- Specification developer
- First device listed
- June 16, 2025
- Registered through
- 2026
- Brand names listed
- StimOn Pain Relief System (GM2439)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 26, 2022 | K213802 | StimOnTM Pain Relief System (GM2439) | GZJ | Substantially Equivalent | Gimer Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 26, 2022. 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.