Skip to content

Guilin Fourth Latex Plant

ChinaFDA applicant, unverified

Devices
1

What Guilin Fourth Latex Plant makes

Guilin Fourth Latex Plant manufactures patient examination gloves, which are single-use barrier devices designed for medical and clinical examinations to reduce cross-contamination risk.

The company’s gloves are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer 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 K893162

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

Frequently asked questions

How many devices does Guilin Fourth Latex Plant have in the registry?

The registry currently lists 1 device for Guilin Fourth Latex Plant. Devices recorded under merged duplicate company entries are counted once.

Which registries list Guilin Fourth Latex Plant's devices?

Among its 1 most recently registered device, Guilin Fourth Latex Plant has devices listed in FDA 510(k) (1 device).

What risk classes do Guilin Fourth Latex Plant's devices fall under?

Among its 1 most recently registered device, the classes recorded for Guilin Fourth Latex Plant's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Guilin Fourth Latex Plant in the registry?

The most recently registered devices listed for Guilin Fourth Latex Plant include PATIENT EXAMINATION GLOVES.

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