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Weco

Country not established

Devices
1

What Weco makes

Weco manufactures Struva and Medi, which are medical devices designed for urinary stone management and prevention, including dissolution and fragmentation therapies.

These devices are classified as Class I under FDA regulations and are listed via 510(k) clearance. 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

  • Struva & Medi Ref K811173

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

Frequently asked questions

How many devices does Weco have in the registry?

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

Which registries list Weco's devices?

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

What risk classes do Weco's devices fall under?

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

What are the newest devices from Weco in the registry?

The most recently registered devices listed for Weco include STRUVA & MEDI.

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