Skip to content

Urocor, Inc.

Country not established

Devices
1

What Urocor, Inc. makes

Urocor, Inc. manufactures radioactive iodine-125 brachytherapy seeds, including the Model 125SL and 125SH, designed for interstitial radiation therapy.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

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

The registry currently lists 1 device for Urocor, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Urocor, Inc.'s devices?

Among its 1 most recently registered device, Urocor, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Urocor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Urocor, Inc. include `BI I-125 BRACHYTHERAPHY SEED, MODEL 125SL & 125SH.

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