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Grand Work Plastic Products Co., Ltd.

US

Last updated May 30, 2026

Part of Grand Work Plastic Products Co., Ltd.

What Grand Work Plastic Products Co., Ltd. makes

Grand Work Plastic Products Co., Ltd. manufactures nitrile and vinyl examination and treatment gloves, both in non-powdered formulations. The nitrile gloves are also non-antimicrobial, designed for medical examinations and procedures requiring barrier protection.

The company’s products are classified as Class I devices under FDA regulations 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 Grand Work Plastic Products Co., Ltd. manufacture?

Grand Work Plastic Products Co., Ltd. specializes in manufacturing nitrile and vinyl examination and treatment gloves. The nitrile gloves are non-powdered and non-antimicrobial, while the vinyl gloves are also non-powdered. These gloves are designed for medical examinations and procedures where barrier protection is required.

Where is Grand Work Plastic Products Co., Ltd. based?

Grand Work Plastic Products Co., Ltd. is based in the United States. The company’s location is relevant for understanding its regulatory environment and manufacturing operations.

Which regulatory registries list Grand Work Plastic Products Co., Ltd.’s devices?

Grand Work Plastic Products Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring traceability and compliance.

How are Grand Work Plastic Products Co., Ltd.’s devices classified under FDA regulations?

Grand Work Plastic Products Co., Ltd.’s gloves are classified as Class I devices under FDA regulations. Class I devices are generally considered to pose the lowest risk and typically require less regulatory oversight, though they still must meet specific performance and safety standards.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
hongray.com.cn
LinkedIn
—
Facebook
—
Email
[email protected]
Phone
+8631166179668
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
527852220

Catalogue (34)

DeviceModel / ReferenceRegistriesClassStatus
Hongray S
FDA UDI
Class IActive
Hongray S
FDA UDI
Class IActive
Hongray L
FDA UDI
Class IActive
Hongray L
FDA UDI
Class IActive
Hongray XXL
FDA UDI
Class IActive
Hongray XL
FDA UDI
Class IActive
Hongray S
FDA UDI
Class IActive
Hongray S
FDA UDI
Class IActive
Hongray XL
FDA UDI
Class IActive
Hongray L
FDA UDI
Class IActive
Hongray XS
FDA UDI
Class IActive
Hongray M
FDA UDI
Class IActive
Hongray XXL
FDA UDI
Class IActive
Hongray XXL
FDA UDI
Class IActive
Hongray M
FDA UDI
Class IActive
Hongray M
FDA UDI
Class IActive
Hongray L
FDA UDI
Class IActive
Hongray XL
FDA UDI
Class IActive
Hongray XXL
FDA UDI
Class IActive
Hongray M
FDA UDI
Class IActive
Hongray S
FDA UDI
Class IActive
Hongray L
FDA UDI
Class IActive
Hongray XS
FDA UDI
Class IActive
Hongray XS
FDA UDI
Class IActive
Hongray XL
FDA UDI
Class IActive
Hongray XS
FDA UDI
Class IActive
Hongray XS
FDA UDI
Class IActive
Hongray M
FDA UDI
Class IActive
Hongray S
FDA UDI
Class IActive
Hongray XL
FDA UDI
Class IActive
Hongray XXL
FDA UDI
Class IActive
Hongray XXL
FDA UDI
Class IActive
Hongray XL
FDA UDI
Class IActive
Hongray XS
FDA UDI
Class IActive

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