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Cathlab Corp.

United StatesFDA applicant, unverified

Devices
8

What Cathlab Corp. makes

Cathlab Corp. manufactures embolic and vascular catheters, including modified embolectomy catheters, silicone arterial embolectomy catheters, and irrigation embolectomy catheters in 3F and 4F sizes. The company also produces silicone occlusion and biliary balloon catheters, silicone flow-directed thermodilution catheters, and percutaneous angiographic/scoping irrigation catheters, including bi-lumen irrigation embolectomy catheters.

All devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. Cathlab Corp. is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

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

The registry currently lists 8 devices for Cathlab Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cathlab Corp.'s devices?

Among its 8 most recently registered devices, Cathlab Corp. has devices listed in FDA 510(k) (8 devices).

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

Among its 8 most recently registered devices, the classes recorded for Cathlab Corp.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Cathlab Corp. include EMBOLECTOMY CATHETER(MODIFIED), CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETER, 3F AND 4F IRRIGATION EMBOLECTOMY CATHETERS and CATHLAB SILICONE OCCLUSION BALLOON CATHETER.

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