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Ken FA Latex Products Corp.

ChinaFDA applicant, unverified

Devices
1

What Ken FA Latex Products Corp. makes

Ken FA Latex Products Corp. manufactures latex examination gloves, designed for single-use medical and clinical applications to maintain hygiene and barrier protection during procedures.

The company’s product portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) pathway 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

  • Latex Examination Gloves Ref K893450

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

Frequently asked questions

How many devices does Ken FA Latex Products Corp. have in the registry?

The registry currently lists 1 device for Ken FA Latex Products Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ken FA Latex Products Corp.'s devices?

Among its 1 most recently registered device, Ken FA Latex Products Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Ken FA Latex Products Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Ken FA Latex Products Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Ken FA Latex Products Corp. in the registry?

The most recently registered devices listed for Ken FA Latex Products Corp. include LATEX EXAMINATION GLOVES.

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