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Zaxis, Inc.

Country not established

Devices
1

What Zaxis, Inc. makes

Zaxis, Inc. manufactures the LFS Lipogel Assay Kit, a diagnostic test designed to measure lipogels in biological samples, likely for clinical or research applications.

This product is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Lfs Lipogel Assay Kit Ref K960785

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

Frequently asked questions

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

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

Which registries list Zaxis, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Zaxis, Inc. include LFS LIPOGEL ASSAY KIT.

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