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American Microptiks, Inc.

Country not established

Devices
1

What American Microptiks, Inc. makes

American Microptiks, Inc. manufactures arthroscopes, including the AMO ARTHOSCOPE series, designed for minimally invasive joint surgeries and diagnostic procedures.

These devices are classified as Class II under FDA regulations and are 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

  • Amo Arthoscopes Ref K962330

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

Frequently asked questions

How many devices does American Microptiks, Inc. have in the registry?

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

Which registries list American Microptiks, Inc.'s devices?

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

What risk classes do American Microptiks, Inc.'s devices fall under?

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

What are the newest devices from American Microptiks, Inc. in the registry?

The most recently registered devices listed for American Microptiks, Inc. include AMO ARTHOSCOPES.

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