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Endosonics Corp.

United StatesFDA applicant, unverified

Devices
15

What Endosonics Corp. makes

Endosonics Corp. manufactures intravascular ultrasound imaging systems, diagnostic imaging catheters, and ultrasonic imaging catheters. The company also produces pressure monitor catheters, PTA balloon dilatation catheters, and automatic pull back devices.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) regulatory registry. The company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Endosonics Corp. have in the registry?

The registry currently lists 15 devices for Endosonics Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Endosonics Corp.'s devices?

Among its 15 most recently registered devices, Endosonics Corp. has devices listed in FDA 510(k) (15 devices).

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

Among its 15 most recently registered devices, the classes recorded for Endosonics Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Endosonics Corp. in the registry?

The most recently registered devices listed for Endosonics Corp. include CATHSCANNER(R) VISIONS(TM) 3.5F 54700/5.0F 54600, VISIONS 8.2F PV ULTRASONIC IMAGING CATHETER (MODEL 88900), ENDOSONICS TRAK BACK DEVICE and CATHSCANNER II INTRAVASCULAR ULTRASONIC IMAGING SY.

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