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Shijiazhuang Great Vision Plastic Products Co., LT

Country not established

Devices
10

What Shijiazhuang Great Vision Plastic Products Co., LT makes

The company manufactures single-use patient examination gloves made from synthetic powdered or powder-free vinyl, including variants in yellow, blue, and white. These gloves are designed for medical and clinical examinations, providing a barrier between healthcare providers and patients.

The portfolio consists of Class I medical devices, listed under the FDA’s 510(k) pathway. The company is based in the United States, and its products are registered with the FDA for commercial distribution.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Shijiazhuang Great Vision Plastic Products Co., LT have in the registry?

The registry currently lists 10 devices for Shijiazhuang Great Vision Plastic Products Co., LT. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shijiazhuang Great Vision Plastic Products Co., LT's devices?

Among its 10 most recently registered devices, Shijiazhuang Great Vision Plastic Products Co., LT has devices listed in FDA 510(k) (10 devices).

What risk classes do Shijiazhuang Great Vision Plastic Products Co., LT's devices fall under?

Among its 10 most recently registered devices, the classes recorded for Shijiazhuang Great Vision Plastic Products Co., LT's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Shijiazhuang Great Vision Plastic Products Co., LT in the registry?

The most recently registered devices listed for Shijiazhuang Great Vision Plastic Products Co., LT include POWDER FREE (BLUE) NITRILE PATIENT EXAMINATION GLOVES, SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES, POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES and POWDER FREE VINYL PATIENT EXAMINATION GLOVES.

Generated automatically from registry data and not verified by a human reviewer.