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.
Catalogue
Search and filter all 164 devicesShowing 1-50 of 164
Frequently asked questions
How many devices does Quinton, Inc. have in the registry?
The registry currently lists 164 devices for Quinton, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Quinton, Inc.'s devices?
Among its 50 most recently registered devices, Quinton, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Quinton, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Quinton, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Quinton, Inc. in the registry?
The most recently registered devices listed for Quinton, Inc. include QUINTON SINGLE LUMEN CATHETER, STAINLESS STEEL GUIDE WIRE, MEDTRACK TREADMILL and PATIENT BY-PASS.