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Angiomedics, Inc.

United StatesFDA applicant, unverified

Devices
8

What Angiomedics, Inc. makes

Angiomedics, Inc. manufactures intravascular catheters and related devices for coronary and peripheral vascular procedures, including percutaneous transluminal angioplasty (PTA) introducers with hemostasis valves, coronary sinus cardioplegia catheters, and diagnostic intravascular catheters. The portfolio also includes angioplasty catheters, sheaths for vascular access, and balloon inflation devices for vascular interventions.

The company’s devices are classified under Class II in the U.S. regulatory framework and are listed via FDA 510(k) clearance. Products are intended for use in interventional cardiology and vascular surgery procedures, adhering to U.S. medical device regulations. The manufacturer is based in the United States.

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

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

How many devices does Angiomedics, Inc. have in the registry?

The registry currently lists 8 devices for Angiomedics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Angiomedics, Inc.'s devices?

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

What risk classes do Angiomedics, Inc.'s devices fall under?

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

What are the newest devices from Angiomedics, Inc. in the registry?

The most recently registered devices listed for Angiomedics, Inc. include SCHNEIDER-SHILEY ANGIOPORT(TM) PTCA INTRO W/HEMO, SOFTIP CORONARY SINUS CARDIOPLEGIA CATHETER, ANGIOMEDIC'S CATHETER-DIAGNOSTIC INTRAVASCULAR and SCHNEIDER-SHILEY SOFTRAC-PTA(TM) ANGIO. CATHETER.

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