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Createch Corp.

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Devices
1

What Createch Corp. makes

Createch Corp. manufactures the KnightWatch System, a medical device designed for continuous monitoring of patients in clinical or home settings, providing real-time alerts and data tracking for respiratory and cardiac parameters.

The KnightWatch System is classified as a Class II 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, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Knightwatch System Ref K896934

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

Frequently asked questions

How many devices does Createch Corp. have in the registry?

The registry currently lists 1 device for Createch Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Createch Corp.'s devices?

Among its 1 most recently registered device, Createch Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Createch Corp.'s devices fall under?

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

What are the newest devices from Createch Corp. in the registry?

The most recently registered devices listed for Createch Corp. include KNIGHTWATCH SYSTEM.

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