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Stanco Medical, Inc.

United StatesFDA applicant, unverified

Devices
19

What Stanco Medical, Inc. makes

Stanco Medical, Inc. manufactures disposable medical kits and components for vascular access, anesthesia delivery, and temporary cardiac pacing. Products include contrast delivery spike kits, regional intravenous anesthesia kits, wireguides for vascular catheters, and complete trays for central venous pressure monitoring. Temporary transvenous pacemaker electrodes and pacing electrode kits are also part of the portfolio, along with stopcocks, pressure monitoring lines, and balloon catheter introduction kits for right atrial access.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded via the 510(k) pathway. These products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

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

The registry currently lists 19 devices for Stanco Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Stanco Medical, Inc.'s devices?

Among its 19 most recently registered devices, Stanco Medical, Inc. has devices listed in FDA 510(k) (19 devices).

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

Among its 19 most recently registered devices, the classes recorded for Stanco Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Stanco Medical, Inc. include DISPOSABLE CONSTRAST DELIVERY SPIKE KIT, REGIONAL INTRAVENOUS ANESTHESIA KIT, VASCULAR CATHETER WIREGUIDES and SWAN GANZ CATHETER PLACEMENT KIT.

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