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Heartland Medical Systems, Inc.

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Devices
1

What Heartland Medical Systems, Inc. makes

Heartland Medical Systems, Inc. manufactures the TRACER, a medical device designed for patient monitoring and tracking within healthcare facilities.

The TRACER is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Tracer Ref K982617

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

Frequently asked questions

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

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

Which registries list Heartland Medical Systems, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Heartland Medical Systems, Inc. include TRACER.

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