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Vance Products, Inc.

United StatesFDA applicant, unverified

Devices
17

What Vance Products, Inc. makes

Vance Products, Inc. manufactures diagnostic and procedural devices for urological and renal applications, including cystoscopes, kidney biopsy brushes, urostomy appliances, and urethral dilation sets. Their portfolio also includes specialized catheters—such as illuminated and deflectable biopsy brushes—and forceps for tissue sampling, as well as ureteral dilation balloons and cystourethrogram sets for imaging procedures.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.

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

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Frequently asked questions

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

The registry currently lists 17 devices for Vance Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vance Products, Inc.'s devices?

Among its 17 most recently registered devices, Vance Products, Inc. has devices listed in FDA 510(k) (17 devices).

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

Among its 17 most recently registered devices, the classes recorded for Vance Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Vance Products, Inc. include VANCE CYSTOSCOPIC, VANCE KIDNEY BIOPSY BRUSHES, VANCE UROSTOMY APPLIANCE and POLLACK CHAIN CYSOURETHROGRAM SET.

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