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Alertronics, Inc.

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Devices
1

What Alertronics, Inc. makes

Alertronics, Inc. manufactures the ALERT BED ALARM SYSTEM, a Class I medical device designed to provide audible and visual alerts for patient positioning or movement within a hospital bed.

The company’s product portfolio is regulated under the FDA’s 510(k) clearance process and is listed in the United States. The device falls under Class I classification.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Alert Bed Alarm System Ref K901969

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

Frequently asked questions

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

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

Which registries list Alertronics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Alertronics, Inc. include ALERT BED ALARM SYSTEM.

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