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Sign in to claim this brandMustech Electronics Co., Limited
US
Last updated May 30, 2026
What Mustech Electronics Co., Limited makes
Mustech Electronics Co., Limited manufactures home-use intense pulsed light (IPL) devices designed for hair removal. These devices are intended for non-invasive treatment of unwanted hair on the skin through targeted light energy.
The company’s IPL hair removal units fall under FDA Class II regulation and are listed via the 510(k) and UDI pathways in the United States. The devices are authorised for commercial distribution through these regulatory mechanisms.
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 Mustech Electronics Co., Limited primarily manufacture?
Mustech Electronics Co., Limited specialises in home-use intense pulsed light (IPL) hair removal units. These devices are designed to target and remove unwanted hair on the skin using controlled light energy, making them suitable for at-home use.
Where is Mustech Electronics Co., Limited based?
Mustech Electronics Co., Limited is based in the United States. The company’s regulatory listings and device classifications reflect its operations within the US market.
Which regulatory registries or databases list Mustech Electronics Co., Limited’s devices?
Mustech Electronics Co., Limited’s devices are listed in the FDA’s 510(k) and UDI registries. These pathways are used to demonstrate compliance and authorisation for Class II devices in the United States.
How are Mustech Electronics Co., Limited’s devices classified under US regulations?
Mustech Electronics Co., Limited’s IPL hair removal units fall under FDA Class II classification. This classification is based on their intended use—non-invasive, low-to-moderate-risk devices requiring special controls beyond general controls to ensure safety and effectiveness.
Why are Mustech Electronics Co., Limited’s devices authorised through the 510(k) and UDI pathways?
The 510(k) pathway is used to demonstrate that a device is substantially equivalent to a legally marketed predicate device, ensuring it meets FDA safety and performance standards. The UDI (Unique Device Identification) system is required for Class II devices to improve tracking, reduce medical errors, and enhance post-market surveillance. Both pathways are necessary for Mustech’s IPL devices to be legally distributed in the US.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- mustech.com
- —
- —
- [email protected]
- Phone
- +86-18926540294
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 421369118
Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mustbeaty | M8013 | FDA UDI | Class II | Active |
| Mustbeaty | M7021 | FDA UDI | Class II | Active |
| Mustbeaty | M8022 | FDA UDI | Class II | Active |
| Mustbeaty | M8021 | FDA UDI | Class II | Active |
| Mustbeaty | M8015 | FDA UDI | Class II | Active |
| Mustbeaty | M8012 | FDA UDI | Class II | Active |
| Mustbeaty | M7012 | FDA UDI | Class II | Active |
| Mustbeaty | M7011 | FDA UDI | Class II | Active |
| Mustbeaty | M8025 | FDA UDI | Class II | Active |
| Mustbeaty | M7023 | FDA UDI | Class II | Active |
| Mustbeaty | M8011 | FDA UDI | Class II | Active |
| Mustbeaty | M8023 | FDA UDI | Class II | Active |
| IPL Hair Removal Device (M8011, M8012, M8013, M8015, M8021, M8022, M8023, M8025, M7011, M7012, M7021, M7023) | K250131 | 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.
- Mustech Electronics Co., Limited Shenzhen Guangdong · CN FEI 3014787341