Data / Medical devices / Taiwan / Might Electronic Co., Ltd.
Might Electronic Co., Ltd.: FDA-registered device maker in Xingfeng Township Hsinchu(County), Taiwan, 4 510(k) clearances
Might Electronic Co., Ltd. is registered with the FDA (registration 3035454575) in Xingfeng Township Hsinchu(County), Taiwan. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated November 8, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035454575
- Address
- No. 8, Ln. 51, Jinggong Rd., Xingfeng Township Hsinchu(County), Taiwan, 304034
- Owner or operator
- MIGHT ELECTRONIC CO., LTD. (10092510)
- Roles
- Manufacturer
- First device listed
- January 16, 2025
- Registered through
- 2026
- Brand names listed
- Trunk and limb electrical stimulator to treat headache
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Distal Transcutaneous Electrical Stimulator For Treatment Of Acute Migraine | QGT | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| November 8, 2023 | K232152 | NerivioInfinity | QGT | Substantially Equivalent | Theranica Bioelectronics , Ltd. | accessdata.fda.gov |
| February 6, 2023 | K223169 | Nerivio | QGT | Substantially Equivalent | Theranica Bioelectronics , Ltd. | accessdata.fda.gov |
| January 22, 2021 | K203181 | Nerivio, FGD000075-4.7 | QGT | Substantially Equivalent | Theranica Bioelectronics , Ltd. | accessdata.fda.gov |
| May 20, 2019 | DEN180059 | Nerivio Migra | QGT | Unknown | Theranica Bioelectronics , Ltd. | accessdata.fda.gov |
Updated November 8, 2023. 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.