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Sign in to claim this brandDongguan Tiger&Rose Technology Limited
US
Last updated May 31, 2026
What Dongguan Tiger&Rose Technology Limited makes
Dongguan Tiger&Rose Technology Limited manufactures blue, red, and infrared phototherapy lamps designed for therapeutic light treatment applications. These devices are intended to deliver targeted light wavelengths for medical or clinical use, such as wound healing, pain management, or skin conditions.
The company’s phototherapy lamps fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The devices are based in the US, adhering to applicable US regulatory standards for medical lighting equipment.
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 Tiger&Rose Technology Limited manufacture?
Dongguan Tiger&Rose Technology Limited specializes in phototherapy lamps that emit blue, red, and infrared light. These devices are designed for therapeutic applications such as wound healing, pain relief, and treatment of skin conditions. The company focuses exclusively on medical lighting solutions, ensuring compliance with relevant standards for phototherapy equipment.
Where is Dongguan Tiger&Rose Technology Limited based, and how does this affect its devices?
The company is based in the US, which means its devices are developed and marketed in accordance with US regulatory requirements. This includes adherence to FDA guidelines for medical devices, ensuring safety, performance, and compliance with applicable standards for phototherapy lamps in the US market.
Which regulatory registries list the devices made by Dongguan Tiger&Rose Technology Limited?
The company’s phototherapy lamps are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices under FDA oversight, ensuring transparency and traceability for Class II devices like those produced by Tiger&Rose.
How are the devices manufactured by Dongguan Tiger&Rose Technology Limited classified under FDA regulations?
The phototherapy lamps produced by Dongguan Tiger&Rose Technology Limited fall under FDA Class II classification. This classification is assigned based on the device’s intended use and risk level, requiring special controls beyond general controls to ensure safety and effectiveness for therapeutic light treatment applications.
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
- 703811456
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tiger&Rose | TR-F08 | FDA UDI | Class II | Active |
| Sharper Image | 1019359 | FDA UDI | Class II | Unknown |
| Sharper Image | 1019498 | FDA UDI | Class I | Unknown |
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