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Thomas J. Fogarty, M.D.

Country not established

Devices
6

What Thomas J. Fogarty, M.D. makes

The company manufactures coaxial balloon dilators for urethral and gastrointestinal use, including devices for treating strictures in the esophagus and urethra. It also produces transluminal endarterectomy tools for vascular procedures and Fogarty occluder pads for vascular occlusion. Additional offerings include gastrointestinal dilators and an oscillometric pulse detection device for monitoring blood pressure.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Thomas J. Fogarty, M.D. have in the registry?

The registry currently lists 6 devices for Thomas J. Fogarty, M.D.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Thomas J. Fogarty, M.D.'s devices?

Among its 6 most recently registered devices, Thomas J. Fogarty, M.D. has devices listed in FDA 510(k) (6 devices).

What risk classes do Thomas J. Fogarty, M.D.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Thomas J. Fogarty, M.D.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Thomas J. Fogarty, M.D. in the registry?

The most recently registered devices listed for Thomas J. Fogarty, M.D. include COAXIAL BALLOON URETHRAL DILATOR, COAXIAL BALLOON GASTROESOPHAGEAL DILA, TRANSLUMINAL ENDARTERECTOMY DEVICE and FOGARTY OCCLUDER PAD.

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