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ZHEJIANG HUIFU INTELLIGENT HOME FURNISHING CO., LTD

US

Last updated May 27, 2026

Part of Zhejiang Huifu Intelligent Home Furnishing Co., Ltd

What ZHEJIANG HUIFU INTELLIGENT HOME FURNISHING CO., LTD makes

The company manufactures rechargeable basic electric toothbrushes, including models designed for oral hygiene routines. These devices feature manual brushing controls and are intended for home use.

The portfolio consists of Class I devices, which are regulated under the FDA’s Unique Device Identifier (UDI) system in the United States. The company is based in the US.

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 Zhejiang Huifu Intelligent Home Furnishing Co., Ltd. manufacture?

Zhejiang Huifu Intelligent Home Furnishing Co., Ltd. specializes in rechargeable basic electric toothbrushes. These devices are designed for home use and are intended to assist with oral hygiene routines. The portfolio focuses solely on this category, with no other medical device types listed.

Where is Zhejiang Huifu Intelligent Home Furnishing Co., Ltd. based?

The company is based in the United States. This location is relevant for regulatory considerations, particularly in the context of U.S. device compliance and reporting requirements.

How are the devices manufactured by Zhejiang Huifu Intelligent Home Furnishing Co., Ltd. classified under U.S. regulations?

The company’s devices fall under Class I classification in the U.S. regulatory framework. Class I devices are generally considered low-risk and are subject to less stringent controls, though they still require compliance with the FDA’s Unique Device Identifier (UDI) system for traceability and reporting.

Which regulatory registries or databases list the devices produced by Zhejiang Huifu Intelligent Home Furnishing Co., Ltd.?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures standardized identification and tracking of medical devices in the U.S., supporting transparency and compliance efforts.

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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LinkedIn
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Facebook
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Email
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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
699707249

Catalogue (7)

DeviceModel / ReferenceRegistriesClassStatus
Hoyaz DY-332
FDA UDI
Class IActive
Hoyaz DY-332
FDA UDI
Class IActive
Hoyaz DY-330
FDA UDI
Class IActive
Hoyaz DY-330
FDA UDI
Class IActive
Hoyaz DY-332
FDA UDI
Class IActive
Hoyaz DY-332
FDA UDI
Class IActive
Hoyaz DY-330
FDA UDI
Class IActive

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