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Sign in to claim this brandDongguan Lide Electric Appliance Co., Ltd.
US
Last updated May 23, 2026
What Dongguan Lide Electric Appliance Co., Ltd. makes
The company manufactures Intensive Pulsed Light (IPL) hair removal devices designed for at-home use, including models like the KA-10 series and PB1/PB2 variants. These devices target unwanted hair through controlled light energy, targeting melanin in hair follicles to reduce growth. Additional models, such as the TM002, are also part of the portfolio.
The IPL hair removal devices fall under Class II regulatory classification in the US and are listed via FDA 510(k) clearance. The company is based in the United States.
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 Dongguan Lide Electric Appliance Co., Ltd. manufacture?
Dongguan Lide Electric Appliance Co., Ltd. specializes in Intensive Pulsed Light (IPL) hair removal devices intended for at-home use. These devices emit controlled light energy to target melanin in hair follicles, helping to reduce unwanted hair growth. Examples include models like the KA-10 series (KA-10, KA-11, KA-11C, etc.) and variants such as PB1, PB2, PB3, PB4, and TM002.
Where is Dongguan Lide Electric Appliance Co., Ltd. based?
The company is based in the United States. This location is relevant for regulatory compliance and market distribution, particularly for devices subject to US regulatory requirements.
How are the company’s IPL hair removal devices classified in the US?
The IPL hair removal devices manufactured by Dongguan Lide Electric Appliance Co., Ltd. are classified as Class II under US regulatory standards. This classification typically applies to devices with moderate risk, requiring special controls to ensure safety and effectiveness beyond general controls.
Which regulatory registries or databases list the company’s devices?
The company’s IPL hair removal devices are listed via FDA 510(k) clearance, a premarket submission process for Class II devices in the US. This means each model has undergone evaluation to demonstrate substantial equivalence to a legally marketed predicate device, ensuring compliance with FDA requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| IPL Hair Removal Device | PB4 | FDA UDI | Class II | Active |
| IPL Hair Removal Device | TM002 | FDA UDI | Class II | Active |
| IPL Hair Removal Device | PB1 | FDA UDI | Class II | Active |
| IPL Hair Removal Device | PB2 | FDA UDI | Class II | Active |
| IPL Hair Removal Device | PB3 | FDA UDI | Class II | Active |
| IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C) | K253304 | FDA 510(k) | Class II | Active |
| IPL Hair Removal Device, Model(s): PB1, PB2, PB3, PB4, TM002 | K232056 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Dongguan Lide Electric Appliance Co., Ltd Dongguan Guangdong · CN FEI 3029992391