Data / Medical devices / China / Shenzhen Minghuangda Electronics Co.,LTD
Shenzhen Minghuangda Electronics Co.,LTD: FDA-registered device maker in Shenzhen Guangdong, China, 2 510(k) clearances
Shenzhen Minghuangda Electronics Co.,LTD is registered with the FDA (registration 3010485091) in Shenzhen Guangdong, China. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated September 9, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010485091
- Address
- Floor 6, Building A, Taixinglong Industrial Park Hezhou Village, Xixiang Town, Baoan District, Shenzhen Guangdong, China, 518100
- Owner or operator
- Shenzhen Minghuangda Electronics Co.,LTD (10061384)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- October 14, 2019
- Registered through
- 2026
- Brand names listed
- EMS Muscle Stimulator, MH-100B, EMS Muscle Stimulator, MH-1038, MH-1048, Foot massager, MH-1019, MHD TENS, MH-1080, MH-1083, MH-1085, MH-1088,MH-100B, TENS & EMS Stimulator, MHD-1083, MH-1080, MH-1083, MH-1087, MH-1036, foot massager (MH-1019)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, Over-The-Counter | NUH | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| September 9, 2024 | K241678 | TENS & EMS Stimulator (MHD-1083) | NUH | Substantially Equivalent | Shenzhen Minghuangda Electronics Co., Ltd. | accessdata.fda.gov |
| June 19, 2019 | K190115 | MHD TENS | NUH | Substantially Equivalent | Minghuangda Electronic Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
- All makers of Stimulator, Nerve, Transcutaneous, Over-The-Counter
Updated September 9, 2024. 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.