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Sign in to claim this brandShenzhen Yihong Lighting Co., Ltd.
US
Last updated May 23, 2026
What Shenzhen Yihong Lighting Co., Ltd. makes
The company manufactures blue, red, and infrared phototherapy lamps designed for medical applications, including the Cabpay series. These devices are intended for therapeutic light exposure treatments, such as neonatal jaundice management or wound healing support.
The portfolio consists of Class II medical devices, listed in the FDA’s Unique Device Identifier (UDI) database. The company operates with a US-based presence, adhering to applicable regulatory requirements for these device classifications.
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 Shenzhen Yihong Lighting Co., Ltd. manufacture?
Shenzhen Yihong Lighting Co., Ltd. specializes in phototherapy lamps that emit blue, red, and infrared light for medical use. These devices are primarily designed for therapeutic applications such as treating neonatal jaundice or supporting wound healing. The company’s portfolio is focused on this single category of Class II devices, specifically the Cabpay series.
Where is Shenzhen Yihong Lighting Co., Ltd. based, and how does this affect its regulatory compliance?
The company has a US-based presence, which means it operates under the regulatory framework of the United States. Since its devices fall under Class II classification, they are subject to FDA requirements, including registration, listing, and compliance with quality system regulations. The US presence also ensures alignment with FDA’s Unique Device Identifier (UDI) system, where these devices are listed.
Which regulatory registries or databases list Shenzhen Yihong Lighting Co., Ltd.’s devices?
Shenzhen Yihong Lighting Co., Ltd.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for commercial distribution in the US, ensuring traceability and compliance with regulatory standards.
How are Shenzhen Yihong Lighting Co., Ltd.’s devices classified under medical device regulations?
The company’s devices, such as the Cabpay series, are classified as Class II medical devices. This classification is determined by the FDA based on the level of risk associated with the device’s intended use. Class II devices generally require special controls in addition to general controls to ensure their safety and effectiveness, and they are subject to mandatory registration and listing 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
- 710198401
Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cabpay | YD003 | FDA UDI | Class II | Active |
| Cabpay | YD056 | FDA UDI | Class II | Active |
| Cabpay | YD015 | FDA UDI | Class II | Active |
| Cabpay | YD002 | FDA UDI | Class II | Active |
| Cabpay | YD001 | FDA UDI | Class II | Active |
| Cabpay | YD079 | FDA UDI | Class II | Active |
| Cabpay | YD001 | FDA UDI | Class II | Active |
| Cabpay | YD007 | FDA UDI | Class II | Active |
| Cabpay | YD001 | FDA UDI | Class II | Active |
| Cabpay | YD001 | FDA UDI | Class II | Active |
| Cabpay | YD050 | FDA UDI | Class II | Active |
| Cabpay | YD013 | FDA UDI | Class II | Active |
| Yihong | YD001 | FDA UDI | Class II | Active |
| Cabpay | YD050 | FDA UDI | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Shenzhen Yihong Lighting Co., Ltd. Shenzhen Guangdong · CN FEI 3017208137