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Quinton, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
164

What Quinton, Inc. makes

Quinton, Inc. manufactures cardiac rehabilitation equipment, including treadmills and imaging/ergometer tables for stress testing, as well as cardiovascular access devices like sheaths, dilators, and catheter systems for interventional procedures. The company also produces patient monitoring tools, such as continuous infusion sets and vital statistics systems for hemodynamic assessment. Electrode systems for cardiac monitoring and vessel tips for vascular access are part of its portfolio.

The company’s devices are classified under FDA’s Class I and Class II categories, with many authorised through the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, reflecting their regulatory clearance status. Quinton, Inc. is headquartered in the United States.

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

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