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Intra Luminal Therapeutics, Inc.

United StatesFDA applicant, unverified

Devices
20

What Intra Luminal Therapeutics, Inc. makes

Intra Luminal Therapeutics, Inc. manufactures coronary and peripheral vascular catheters, guide wires, and radiofrequency total occlusion crossing systems designed for crossing chronic total occlusions. Their portfolio includes deflecting catheters, torquers, and support catheters, all intended for use in percutaneous coronary and peripheral interventions.

The company’s devices are classified as Class II under FDA regulations and are recorded in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.

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

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Frequently asked questions

How many devices does Intra Luminal Therapeutics, Inc. have in the registry?

The registry currently lists 20 devices for Intra Luminal Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Intra Luminal Therapeutics, Inc.'s devices?

Among its 20 most recently registered devices, Intra Luminal Therapeutics, Inc. has devices listed in FDA 510(k) (20 devices).

What risk classes do Intra Luminal Therapeutics, Inc.'s devices fall under?

Among its 20 most recently registered devices, the classes recorded for Intra Luminal Therapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Intra Luminal Therapeutics, Inc. in the registry?

The most recently registered devices listed for Intra Luminal Therapeutics, Inc. include ILT 0.014 CATHETER, MODEL C114NL2, SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM [CORONARY], ILT DEFLECTING CATHETER, MODEL C114ND1 and SAFE-CROSS DEFLECTING CATHETER, MODEL C118ND1.

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