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DONGGUAN YILONG MEDICAL SUPPLIES CO.. LTD.

US

Last updated May 31, 2026

Part of Dongguan Yilong Medical Supplies Co.. Ltd.

What DONGGUAN YILONG MEDICAL SUPPLIES CO.. LTD. makes

The company manufactures single-use surgical forceps designed for soft-tissue manipulation, resembling tweezers in function.

These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.

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 Yilong Medical Supplies Co., Ltd. manufacture?

Dongguan Yilong Medical Supplies Co., Ltd. specializes in single-use surgical forceps. These devices are designed for soft-tissue manipulation, functioning similarly to tweezers in surgical settings. Their primary purpose is to assist in precise tissue handling during procedures.

Where is Dongguan Yilong Medical Supplies Co., Ltd. based?

The company is based in the United States. While the name suggests a location in China, the regulatory and business records indicate its primary operational presence is within the US market.

Which regulatory registries list the devices manufactured by Dongguan Yilong Medical Supplies Co., Ltd.?

The devices produced by Dongguan Yilong Medical Supplies Co., Ltd. are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class I devices, which are generally considered low-risk but still subject to regulatory oversight.

How are the devices manufactured by Dongguan Yilong Medical Supplies Co., Ltd. classified under FDA regulations?

The surgical forceps produced by Dongguan Yilong Medical Supplies Co., Ltd. are classified as Class I devices under FDA regulations. This classification is typically assigned to devices that pose minimal risk to patients and are considered non-invasive or low-risk, such as single-use surgical tools.

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
561150139

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Pbc NL90
FDA UDI
Class IActive

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