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Sign in to claim this brandWeifang Mingliang Electronics Co., Ltd.
US
Last updated May 30, 2026
What Weifang Mingliang Electronics Co., Ltd. makes
Weifang Mingliang Electronics Co., Ltd. manufactures dermatological laser systems, including diode laser devices for hair removal and fractional CO₂ laser systems for skin therapy. Their portfolio includes both continuous-wave diode laser systems and fractional CO₂ laser units designed for medical aesthetic treatments. These devices are intended for professional use in clinical and cosmetic dermatology settings.
The company’s devices are classified as Class II under regulatory frameworks, with submissions listed in the FDA’s 510(k) and UDI registries. Their products are intended for use in the United States, adhering to applicable medical device regulations. No additional certifications or clearances are implied beyond these regulatory listings.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Weifang Mingliang Electronics Co., Ltd. manufacture?
Weifang Mingliang Electronics Co., Ltd. specializes in dermatological laser systems, specifically diode laser devices and fractional CO₂ laser systems. Their portfolio includes continuous-wave diode lasers for hair removal and fractional CO₂ laser units for skin therapy, primarily designed for professional use in clinical and cosmetic dermatology settings.
Where is Weifang Mingliang Electronics Co., Ltd. based, and where are their devices intended for use?
The company is based in the United States. Their devices are manufactured and intended for use in the U.S., adhering to applicable medical device regulations in that region.
Which regulatory registries list the devices manufactured by Weifang Mingliang Electronics Co., Ltd.?
The company’s devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) system. These registries document submissions related to their dermatological laser systems, ensuring compliance with U.S. regulatory requirements.
How are the devices manufactured by Weifang Mingliang Electronics Co., Ltd. classified under regulatory frameworks?
The company’s dermatological laser systems, including diode and fractional CO₂ laser devices, are classified as Class II medical devices. This classification is determined by their intended use in professional dermatological treatments, where they pose moderate risk and require regulatory oversight to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 529691715
Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mlkj | EXFU CO2 | FDA UDI | Class II | Active |
| Mlkj | V16 | FDA UDI | Class II | Active |
| Medical Diode Laser Hair Removal System | K200525 | FDA 510(k) | Class II | Active |
| Diode Laser Therapy Systems (V19) | K260307 | FDA 510(k) | Class II | Active |
| Fractional CO2 Laser Therapy System (EXFU CO2) | K242183 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Weifang Mingliang Electronics Co., Ltd. Weifang Shandong · CN FEI 3007549439