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Shanghai PT Plastics Enterprise Company, Ltd.

ChinaFDA applicant, unverified

Devices
6

What Shanghai PT Plastics Enterprise Company, Ltd. makes

The company manufactures disposable synthetic medical gloves, including powder-free vinyl and PVC examination gloves. Variants include standard white vinyl gloves, aloe vera-infused green vinyl gloves, and powdered PVC gloves. These products are designed for patient examinations and medical procedures.

The portfolio consists of Class I medical devices, regulated under the FDA’s 510(k) clearance pathway. Products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

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

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Shanghai PT Plastics Enterprise Company, Ltd. have in the registry?

The registry currently lists 6 devices for Shanghai PT Plastics Enterprise Company, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shanghai PT Plastics Enterprise Company, Ltd.'s devices?

Among its 6 most recently registered devices, Shanghai PT Plastics Enterprise Company, Ltd. has devices listed in FDA 510(k) (6 devices).

What risk classes do Shanghai PT Plastics Enterprise Company, Ltd.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Shanghai PT Plastics Enterprise Company, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Shanghai PT Plastics Enterprise Company, Ltd. in the registry?

The most recently registered devices listed for Shanghai PT Plastics Enterprise Company, Ltd. include PT SYNTHETIC MEDICAL GLOVES, POWDER FREE, DISPOSABLE PVC SYNTHETIC EXAMINATION GLOVES, POWDER FREE, DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES, WHITE COLOR and DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES WITH ALOE VERA, GREEN COLOR.

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