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Centauri Medical, Inc.

Country not established

Devices
1

What Centauri Medical, Inc. makes

Centauri Medical, Inc. manufactures the DYNASENSE SYSTEM, a medical device designed for [specific application not detailed in data]. The system is intended for [intended use or clinical purpose not specified in data].

The DYNASENSE SYSTEM is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) registry. 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

  • Dynasense System Ref K130752

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

Frequently asked questions

How many devices does Centauri Medical, Inc. have in the registry?

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

Which registries list Centauri Medical, Inc.'s devices?

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

What risk classes do Centauri Medical, Inc.'s devices fall under?

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

What are the newest devices from Centauri Medical, Inc. in the registry?

The most recently registered devices listed for Centauri Medical, Inc. include DYNASENSE SYSTEM.

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