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Rd Chus, Inc.

Country not established

Devices
1

What Rd Chus, Inc. makes

Rd Chus, Inc. manufactures the Laparette, a device designed for laparoscopic procedures, likely used for tissue retrieval or specimen containment during minimally invasive surgeries.

The company’s product portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The manufacturer 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

  • Laparette Ref K971146

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

Frequently asked questions

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

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

Which registries list Rd Chus, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Rd Chus, Inc. include LAPARETTE.

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