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Oxford Medilog, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
48

What Oxford Medilog, Inc. makes

Oxford Medilog, Inc. manufactures ambulatory and intensive care monitoring systems, including Holter recorders, electrophysiological monitoring devices, and ambulatory pH monitoring systems. Their products capture and analyze cardiac rhythms, skin temperature, and other physiological signals for diagnostic purposes. The portfolio also includes specialized recorders for ambulatory ECG and patient monitoring systems designed for critical care environments.

The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with many listed via the 510(k) pathway. Products are regulated under US medical device laws and appear in the FDA’s 510(k) database. The manufacturer is based in the United States.

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

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Frequently asked questions

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

The registry currently lists 48 devices for Oxford Medilog, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Oxford Medilog, Inc.'s devices?

Among its 48 most recently registered devices, Oxford Medilog, Inc. has devices listed in FDA 510(k) (48 devices).

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

Among its 48 most recently registered devices, the classes recorded for Oxford Medilog, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Oxford Medilog, Inc. include MEDILOG 2500 SYSTEM, MEDILOG 9000-II AMBULATORY RECORDER, MODEL 5000 AMBULATORY MONITORING SYSTEM and MEDILOG M6.

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