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Sign in to claim this brandZhejiang Hongyu Medicali Commodity Co., Ltd.
US
Last updated May 23, 2026
What Zhejiang Hongyu Medicali Commodity Co., Ltd. makes
Zhejiang Hongyu Medicali Commodity Co., Ltd. manufactures surgical face masks designed for single-use in medical and surgical settings to reduce airborne contamination and infection risk during procedures.
The company’s products are regulated as Class II devices under FDA requirements and are listed via the 510(k) pathway in 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 Zhejiang Hongyu Medicali Commodity Co., Ltd. manufacture?
Zhejiang Hongyu Medicali Commodity Co., Ltd. specializes in surgical face masks. These devices are intended for single-use in medical and surgical environments to help minimize airborne contamination and lower infection risks during procedures. The focus is on products that meet critical hygiene needs in healthcare settings.
Where is Zhejiang Hongyu Medicali Commodity Co., Ltd. based?
The company is based in the United States. While the name suggests an origin in Zhejiang, China, its operational headquarters and regulatory filings are conducted through its US entity, which is relevant for compliance and market access in the US healthcare system.
How are Zhejiang Hongyu Medicali Commodity Co., Ltd.’s devices classified under US regulations?
The company’s devices, such as surgical face masks, are classified as Class II under FDA regulations. This classification applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, including performance standards or post-market surveillance. The classification is determined by the device’s intended use and potential health impact.
Which regulatory registries or databases list Zhejiang Hongyu Medicali Commodity Co., Ltd.’s devices?
Zhejiang Hongyu Medicali Commodity Co., Ltd.’s devices are listed in the FDA’s 510(k) database. The 510(k) pathway is used to demonstrate that a new device is substantially equivalent to a legally marketed predicate device, ensuring compliance with FDA requirements before commercial distribution in the US. This registry provides transparency on device authorizations and regulatory history.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Hongyu | KY5435 | FDA UDI | Class I | Active |
| Surgical Face Mask | K211897 | FDA 510(k) | Class II | Active |
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