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Zibo Daiyang Plastic Company

ChinaFDA 510(k) applicant, unverified

Devices
1

What Zibo Daiyang Plastic Company makes

The company manufactures powder-free vinyl patient examination gloves, specifically clear (non-colored) versions designed for medical use.

These products fall under FDA Class I regulatory classification and are listed via 510(k) clearance in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Zibo Daiyang Plastic Company have in the registry?

The registry currently lists 1 device for Zibo Daiyang Plastic Company. Devices recorded under merged duplicate company entries are counted once.

Which registries list Zibo Daiyang Plastic Company's devices?

Among its 1 most recently registered device, Zibo Daiyang Plastic Company has devices listed in FDA 510(k) (1 device).

What risk classes do Zibo Daiyang Plastic Company's devices fall under?

Among its 1 most recently registered device, the classes recorded for Zibo Daiyang Plastic Company's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Zibo Daiyang Plastic Company in the registry?

The most recently registered devices listed for Zibo Daiyang Plastic Company include DAIYANG Powder Free Vinyl Patient Examination Gloves, Clear (non-colored).

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