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Shen Yunn Plastics Corp.

TaiwanFDA applicant, unverified

Devices
1

What Shen Yunn Plastics Corp. makes

Shen Yunn Plastics Corp. manufactures patient examination gloves, designed for single-use medical procedures requiring barrier protection.

These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based 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

  • Patient Examination Gloves Ref K892998

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Shen Yunn Plastics Corp. have in the registry?

The registry currently lists 1 device for Shen Yunn Plastics Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shen Yunn Plastics Corp.'s devices?

Among its 1 most recently registered device, Shen Yunn Plastics Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Shen Yunn Plastics Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Shen Yunn Plastics Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Shen Yunn Plastics Corp. in the registry?

The most recently registered devices listed for Shen Yunn Plastics Corp. include PATIENT EXAMINATION GLOVES.

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