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Diagnostic Ultrasound Corp.

United StatesFDA applicant, unverified

Devices
16

What Diagnostic Ultrasound Corp. makes

Diagnostic Ultrasound Corp. manufactures portable and handheld diagnostic ultrasound devices, including models specialized for urological and gynecological assessments. Their portfolio includes systems like the BladderManager PCI 5000 and BladderScan BVI 5000 for bladder volume measurement, as well as general diagnostic ultrasound units such as the UDS 2000 Series and VersaDopp 1000. Additional offerings include video-enabled models like the UD 2000 and ultrasound Doppler devices for vascular and obstetric evaluations.

These devices are classified as Class II under FDA regulations and are recorded in the FDA’s 510(k) premarket notification database. The company operates from the United States, where its products are subject to FDA oversight for compliance with medical device authorization requirements.

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 Diagnostic Ultrasound Corp. have in the registry?

The registry currently lists 16 devices for Diagnostic Ultrasound Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diagnostic Ultrasound Corp.'s devices?

Among its 16 most recently registered devices, Diagnostic Ultrasound Corp. has devices listed in FDA 510(k) (16 devices).

What risk classes do Diagnostic Ultrasound Corp.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Diagnostic Ultrasound Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Diagnostic Ultrasound Corp. in the registry?

The most recently registered devices listed for Diagnostic Ultrasound Corp. include BLADDERMANAGER PCI 5000 MODEL 1002, DIAGNOSTIC ULTRASOUND/URO-GYN UD 511, BLADDER MANAGER PCI 5000, BLADDERSCAN BVI 5000 and DIAGNOSTIC ULTRASOUND 105 & 110.

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