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Diasonics, Inc.

United StatesFDA applicant, unverified

Devices
43

What Diasonics, Inc. makes

Diasonics, Inc. manufactures medical imaging equipment and diagnostic accessories, including ultrasound imaging systems, digital fluorographic imaging systems, and color flow mapping systems. Their product line also features specialized probes, such as transrectal and Doppler transducers, as well as magnetic resonance device accessories and stereotactic neurobiopsy equipment.

The company is based in the United States, and its portfolio includes devices classified as Class I and Class II. These products are documented within the FDA 510(k) and PMA regulatory registries.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

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

The registry currently lists 43 devices for Diasonics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diasonics, Inc.'s devices?

Among its 43 most recently registered devices, Diasonics, Inc. has devices listed in FDA 510(k) (42 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.

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

Among its 43 most recently registered devices, the classes recorded for Diasonics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Diasonics, Inc. include DIGITAL FLUROGRAPHIC IMAGING SYSTEM, CW DOPPLER 2.25 MHZ PROBE, DIASONICS DRF-200 ULTRASOUND IMAGING SYSTEM and DIASONICS, BERGER STEREOTACTIC NEOROBIOPSY.

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