Data / Medical devices / China / Weifang Mingliang Electronics Co.,ltd.
Weifang Mingliang Electronics Co.,ltd.: FDA-registered device maker in Weifang Shandong, China, 3 510(k) clearances
Weifang Mingliang Electronics Co.,ltd. is registered with the FDA (registration 3007549439) in Weifang Shandong, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 15, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007549439
- Address
- Building 67, Weifang Yuandu Huizhi Industrial Park, east of Wenhua Road and north of Taixiang, Weifang Shandong, China, 261000
- Owner or operator
- Weifang Mingliang Electronics CO.,LTD. (10082104)
- Roles
- Manufacturer
- First device listed
- June 16, 2021
- Registered through
- 2026
- Brand names listed
- Diode Laser Therapy Systems, Fractional CO2 Laser Therapy System (EXFU CO2), Medical Diode Laser Hair Removal System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument With MicrobeamFractional Output | ONG | 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 |
|---|---|---|---|---|---|---|
| April 15, 2026 | K260307 | Diode Laser Therapy Systems (V19) | GEX | Substantially Equivalent | Weifang Mingliang Electronics Co., Ltd. | accessdata.fda.gov |
| October 23, 2024 | K242183 | Fractional CO2 Laser Therapy System (EXFU CO2) | GEX | Substantially Equivalent | Weifang Mingliang Electronics Co., Ltd. | accessdata.fda.gov |
| May 27, 2020 | K200525 | Medical Diode Laser Hair Removal System | GEX | Substantially Equivalent | Weifang Mingliang Electronics Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Laser Surgical Instrument With MicrobeamFractional Output
Updated April 15, 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.