Skip to content

Circ Medtech

Country not established

Devices
1

What Circ Medtech makes

Circ Medtech manufactures the PREPEX System, a medical device designed for the permanent medical management of male circumcision.

The PREPEX System is classified as a Class II device under FDA regulations and is authorised 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

  • Prepex System Ref K103695

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Circ Medtech have in the registry?

The registry currently lists 1 device for Circ Medtech. Devices recorded under merged duplicate company entries are counted once.

Which registries list Circ Medtech's devices?

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

What risk classes do Circ Medtech's devices fall under?

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

What are the newest devices from Circ Medtech in the registry?

The most recently registered devices listed for Circ Medtech include PREPEX SYSTEM.

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