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Sign in to claim this brandDongguan Fumeikang Electrical Technology Co., Ltd.
US
Last updated May 31, 2026
What Dongguan Fumeikang Electrical Technology Co., Ltd. makes
The company manufactures electric oral hygiene devices, including water jet flossers and sonic electric toothbrushes, designed for at-home dental care. These products use water or sonic vibrations to clean teeth and gums, targeting plaque and interdental spaces.
The portfolio consists of Class I medical devices, which are generally considered low-risk and subject to minimal regulatory oversight. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements.
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 Fumeikang Electrical Technology Co., Ltd. manufacture?
Dongguan Fumeikang Electrical Technology Co., Ltd. specializes in electric oral hygiene devices, including water jet flossers and sonic electric toothbrushes. These devices are designed for at-home use to improve dental care by removing plaque and cleaning interdental spaces using water jets or sonic vibrations.
Where is Dongguan Fumeikang Electrical Technology Co., Ltd. based?
The company is based in the United States, though its manufacturing origins may trace back to its namesake location in Dongguan, China. The U.S. presence is relevant for regulatory compliance and market distribution in North America.
Which regulatory registries list the devices made by Dongguan Fumeikang Electrical Technology Co., Ltd.?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance with U.S. regulatory requirements for medical devices, particularly for Class I products.
How are the devices manufactured by Dongguan Fumeikang Electrical Technology Co., Ltd. classified?
The devices produced by the company fall under Class I classification, which is the lowest risk category for medical devices. This classification typically applies to devices with minimal potential risk to users, such as oral hygiene tools, and requires less stringent regulatory scrutiny compared to higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 529308043
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