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R. Lewis, Inc.

Country not established

Devices
1

What R. Lewis, Inc. makes

R. Lewis, Inc. makes medical devices such as tube holders, including The Lewis Tube Holder.

The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • The Lewis Tube Holder Ref K920691

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

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

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

Which registries list R. Lewis, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for R. Lewis, Inc. include THE LEWIS TUBE HOLDER.

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