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Quantum Medical Systems, Inc.

United StatesFDA applicant, unverified

Devices
5

What Quantum Medical Systems, Inc. makes

Quantum Medical Systems, Inc. manufactures ultrasound systems designed for angiography and vascular assessments, including systems with color Doppler capabilities. Their portfolio includes dedicated angiodyngraph units with interchangeable probes (e.g., 5.0 MHz and 7.5 MHz) for imaging blood flow and vascular structures. These devices are intended for diagnostic evaluation of peripheral and coronary arteries, as well as dynamic blood flow studies.

The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. These devices are listed in the FDA’s 510(k) database, reflecting their regulatory pathway in the United States. The manufacturer operates from the US.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Quantum Medical Systems, Inc. have in the registry?

The registry currently lists 5 devices for Quantum Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Quantum Medical Systems, Inc.'s devices?

Among its 5 most recently registered devices, Quantum Medical Systems, Inc. has devices listed in FDA 510(k) (5 devices).

What risk classes do Quantum Medical Systems, Inc.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for Quantum Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Quantum Medical Systems, Inc. in the registry?

The most recently registered devices listed for Quantum Medical Systems, Inc. include QUANTUM QAD ANGIODYNOGRAPH ULTRASOUND SYSTEM, QAD-1 ANGIO DYNOGRAPH ULTRASO W/5.0 7.5 MHZ PROBES, QUANTUM 2000 ANGIODYNOGRAPH ULTRASOUND SYSTEM and QAD-1 ANGIODYNOGRAPH ULTRASOUND SYSTEM.

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