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Sign in to claim this brandKinreen Technology (Shenzhen) Co., Ltd
US
Last updated May 30, 2026
What Kinreen Technology (Shenzhen) Co., Ltd makes
Kinreen Technology produces non-wearable infrared phototherapy units designed for musculoskeletal applications, including devices like the Lumadoc, ZOOM WELLNESS, and CureBio. These units are intended for therapeutic treatment of muscle and joint conditions through controlled infrared light exposure.
The company’s portfolio consists of Class II medical devices, which are regulated under the FDA’s Unique Device Identification (UDI) system. These devices are listed in the FDA’s UDI database, adhering to U.S. regulatory requirements for Class II products.
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 Kinreen Technology (Shenzhen) Co., Ltd manufacture?
Kinreen Technology specializes in non-wearable musculoskeletal infrared phototherapy units. These devices are designed to deliver controlled infrared light therapy for treating muscle and joint conditions, such as those offered by products like Lumadoc, ZOOM WELLNESS, and CureBio. The focus is on therapeutic applications for pain relief and tissue repair.
Where is Kinreen Technology (Shenzhen) Co., Ltd based?
Kinreen Technology (Shenzhen) Co., Ltd is based in the United States. While the company name includes 'Shenzhen,' its operational headquarters and regulatory presence align with U.S. standards, including compliance with FDA requirements for its devices.
Which regulatory registries list Kinreen Technology’s devices?
Kinreen Technology’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry is required for Class II medical devices in the U.S., ensuring traceability and compliance with regulatory standards for these therapeutic phototherapy units.
How are Kinreen Technology’s devices classified under U.S. regulations?
Kinreen Technology’s devices fall under the FDA’s Class II classification. This classification applies to devices with a moderate level of risk, requiring special controls beyond general controls to ensure safety and effectiveness. Class II devices like their infrared phototherapy units are subject to stricter regulatory oversight, including UDI requirements.
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
- 554534919
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lumadoc | QY-P-DE-R | FDA UDI | Class II | Active |
| Zoom Wellness | QY-S-BD-A | FDA UDI | Class II | Active |
| CureBio | QY-P-DE-R+P | FDA UDI | Class II | Active |
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