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Daesung America Co., Inc.

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Devices
1

What Daesung America Co., Inc. makes

Daesung America Co., Inc. manufactures TIGER Patient Exam Gloves, a type of single-use nitrile examination glove designed for medical and clinical examinations to reduce the risk of contamination and infection.

The company’s portfolio is regulated under FDA Class I devices and is listed via 510(k) clearance. The manufacturer is based in the United States.

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

Catalogue1

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Frequently asked questions

How many devices does Daesung America Co., Inc. have in the registry?

The registry currently lists 1 device for Daesung America Co., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Daesung America Co., Inc.'s devices?

Among its 1 most recently registered device, Daesung America Co., Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Daesung America Co., Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Daesung America Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Daesung America Co., Inc. in the registry?

The most recently registered devices listed for Daesung America Co., Inc. include TIGER PATIENT EXAM GLOVES.

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