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Rota Systems, Inc.

Country not established

Devices
1

What Rota Systems, Inc. makes

Rota Systems, Inc. manufactures the ROTA DATAMATE I, a device designed for data acquisition and processing in medical or research settings, likely for monitoring physiological signals or experimental data collection.

The ROTA DATAMATE I is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) database. 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

  • Rota Datamate I Ref K935945

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

Frequently asked questions

How many devices does Rota Systems, Inc. have in the registry?

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

Which registries list Rota Systems, Inc.'s devices?

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

What risk classes do Rota Systems, Inc.'s devices fall under?

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

What are the newest devices from Rota Systems, Inc. in the registry?

The most recently registered devices listed for Rota Systems, Inc. include ROTA DATAMATE I.

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