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Datrix, Inc. Dba of Jon Barron, Inc.

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Devices
1

What Datrix, Inc. Dba of Jon Barron, Inc. makes

Datrix, Inc. manufactures the E-TAC EX-1000, an electrocardiographic event recorder designed to capture and store cardiac rhythm data for diagnostic evaluation.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The devices are listed in the FDA’s 510(k) database. The company is based in the United States.

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

Catalogue1

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Frequently asked questions

How many devices does Datrix, Inc. Dba of Jon Barron, Inc. have in the registry?

The registry currently lists 1 device for Datrix, Inc. Dba of Jon Barron, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Datrix, Inc. Dba of Jon Barron, Inc.'s devices?

Among its 1 most recently registered device, Datrix, Inc. Dba of Jon Barron, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Datrix, Inc. Dba of Jon Barron, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Datrix, Inc. Dba of Jon Barron, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Datrix, Inc. Dba of Jon Barron, Inc. in the registry?

The most recently registered devices listed for Datrix, Inc. Dba of Jon Barron, Inc. include E-TAC EX-1000 ELECTROCARDIOGRAPHIC EVENT RECORDER.

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