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Oxford Instruments Medical, Ltd.

United KingdomFDA 510(k) applicant, unverified

Devices
1

What Oxford Instruments Medical, Ltd. makes

Oxford Instruments Medical, Ltd. manufactures the SONICAID ONE, a device designed for low-intensity pulsed ultrasound therapy, used primarily for musculoskeletal pain management and tissue repair.

The SONICAID ONE is classified as a Class II medical device and is listed under the FDA’s 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

  • Sonicaid One Ref K023618

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Oxford Instruments Medical, Ltd. have in the registry?

The registry currently lists 1 device for Oxford Instruments Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Oxford Instruments Medical, Ltd.'s devices?

Among its 1 most recently registered device, Oxford Instruments Medical, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Oxford Instruments Medical, Ltd.'s devices fall under?

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

What are the newest devices from Oxford Instruments Medical, Ltd. in the registry?

The most recently registered devices listed for Oxford Instruments Medical, Ltd. include SONICAID ONE.

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