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Yuntek International, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
2

What Yuntek International, Inc. makes

Yuntek International, Inc. manufactures electrosurgical pencils, including surgical and standard models, designed for precise tissue cutting and coagulation in surgical procedures.

These devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

Frequently asked questions

How many devices does Yuntek International, Inc. have in the registry?

The registry currently lists 2 devices for Yuntek International, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Yuntek International, Inc.'s devices?

Among its 2 most recently registered devices, Yuntek International, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Yuntek International, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Yuntek International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Yuntek International, Inc. in the registry?

The most recently registered devices listed for Yuntek International, Inc. include SURGICAL PENCIL/ ELECTROSURGICAL PENCIL and ELECTROSURGICAL PENCIL.

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