Data / Medical devices / China / Mustech Electronics Co., Limited
Mustech Electronics Co., Limited: FDA-registered device maker in Shenzhen Guangdong, China, 1 510(k) clearance
Mustech Electronics Co., Limited is registered with the FDA (registration 3014787341) in Shenzhen Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 19, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014787341
- Address
- 3F, Building No.B2, Shanghe Industry Park, NanChang Road, Xixiang Town, Baoan District, Shenzhen Guangdong, China, 518126
- Owner or operator
- Mustech Electronics Co., Limited (10093068)
- Roles
- Manufacturer
- First device listed
- March 26, 2025
- Registered through
- 2026
- Brand names listed
- IPL Hair Removal Device (Model: M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023), MUSTBEATY (Model: M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023), RaysDanc Pure (Model: M8015)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light Based Over-The-Counter Hair Removal | OHT | 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 |
|---|---|---|---|---|---|---|
| March 19, 2025 | K250131 | IPL Hair Removal Device (M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023) | OHT | Substantially Equivalent | Mustech Electronics Co., Limited | accessdata.fda.gov |
Compare with other makers
Updated March 19, 2025. 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.