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Sign in to claim this brandNingbo Yimei Nikko-seiki Manufacture Co., LTD
US
Last updated May 30, 2026
What Ningbo Yimei Nikko-seiki Manufacture Co., LTD makes
The company manufactures red and infrared light phototherapy units designed for therapeutic applications, including the Quasar MD model.
These devices are classified as Class II under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Ningbo Yimei Nikko-seiki Manufacture Co., LTD produce?
Ningbo Yimei Nikko-seiki Manufacture Co., LTD specializes in red and infrared light phototherapy units. These devices are designed for therapeutic applications, such as pain relief, tissue repair, or inflammation reduction, using controlled light wavelengths. The Quasar MD is an example of their product line.
Where is Ningbo Yimei Nikko-seiki Manufacture Co., LTD based?
The company operates from the United States. While the name suggests a Chinese origin, the manufacturing and business operations are conducted within the US market.
How are the devices produced by Ningbo Yimei Nikko-seiki classified under regulatory standards?
The devices manufactured by Ningbo Yimei Nikko-seiki are classified as Class II under regulatory frameworks. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness.
Are the devices from Ningbo Yimei Nikko-seiki listed in any regulatory registries?
Yes, the company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, clinical, and commercial purposes, ensuring traceability and compliance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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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
- 553152875
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