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King Tool, Inc.

Country not established

Devices
1

What King Tool, Inc. makes

King Tool, Inc. manufactures the Eye See Instrument, a device designed for ophthalmic examinations or diagnostic procedures.

The Eye See Instrument is classified as a Class I medical device under FDA regulations and is listed via 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.

Catalogue1

Newest first, rows 1-1 of 1

  • Eye See Instrument Ref K905237

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

Frequently asked questions

How many devices does King Tool, Inc. have in the registry?

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

Which registries list King Tool, Inc.'s devices?

Among its 1 most recently registered device, King Tool, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do King Tool, Inc.'s devices fall under?

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

What are the newest devices from King Tool, Inc. in the registry?

The most recently registered devices listed for King Tool, Inc. include EYE SEE INSTRUMENT.

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