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Clinical Technologies, Inc.

Country not established

Devices
1

What Clinical Technologies, Inc. makes

Clinical Technologies, Inc. manufactures the CT Spacer, a device designed for use in respiratory therapy to measure inhaled medication dosage accuracy.

The CT Spacer is classified as a Class II 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

  • Ct Spacer Ref K010680

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

Frequently asked questions

How many devices does Clinical Technologies, Inc. have in the registry?

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

Which registries list Clinical Technologies, Inc.'s devices?

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

What risk classes do Clinical Technologies, Inc.'s devices fall under?

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

What are the newest devices from Clinical Technologies, Inc. in the registry?

The most recently registered devices listed for Clinical Technologies, Inc. include CT SPACER.

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