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Sign in to claim this brandChongqing Peninsula Medical Technology Co., Ltd.
US
Last updated May 30, 2026
What Chongqing Peninsula Medical Technology Co., Ltd. makes
The company manufactures laser-based devices for hair growth and professional ultraviolet phototherapy units, including irradiation systems for aesthetic and cosmetic applications. These devices include 308nm excimer systems and handheld aesthetic irradiation tools designed for controlled light therapy.
The portfolio consists of Class II medical devices, authorised through FDA pathways including 510(k) and UDI registrations. The company’s products are listed under US regulatory frameworks and are 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 Chongqing Peninsula Medical Technology Co., Ltd. manufacture?
The company specializes in laser-based medical devices, primarily focusing on hair growth laser systems and professional ultraviolet phototherapy units. Their portfolio includes irradiation devices for aesthetic and cosmetic applications, such as 308nm excimer systems and handheld aesthetic irradiation tools, which use controlled light therapy for targeted treatments.
Where is Chongqing Peninsula Medical Technology Co., Ltd. based?
The company is based in the United States, as indicated in its regulatory documentation. This location is relevant for understanding its compliance with US regulatory frameworks, such as FDA requirements.
Which regulatory registries or pathways are used for the company’s devices in the US?
The company’s devices are listed under the FDA’s regulatory pathways, specifically the 510(k) premarket notification process and Unique Device Identifier (UDI) registrations. These pathways are used to demonstrate that their Class II devices meet applicable safety and performance standards before entering the market.
How are the company’s devices classified under US regulations?
All of Chongqing Peninsula Medical Technology Co., Ltd.’s devices fall under Class II classification in the US. This classification is determined by the FDA based on the level of risk associated with the device’s intended use, requiring special controls beyond general controls 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
- 545832254
Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Irradiation Aesthetic Device | HairPro | FDA UDI | Class II | Active |
| 308nm Excimer System | XECL-308C, XECL-308D | FDA UDI | Class II | Active |
| Irradiation Cosmetic Device | K192552 | FDA 510(k) | Class II | Active |
| 308nm Excimer System | K172273 | FDA 510(k) | Class II | Active |
| 308nm Excimer System | K192642 | FDA 510(k) | Class II | Active |
| Irradiation Aesthetic Device | K171835 | 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.
- Chongqing Peninsula Medical Technology Co., Ltd. Chongqing · CN FEI 3015060197