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Saturn Imaging, Inc.

TaiwanFDA applicant, unverified

Devices
1

What Saturn Imaging, Inc. makes

Saturn Imaging, Inc. makes ImplantMax Software.

The company's device is classified as Class II and is listed in the FDA 510(k) registry. 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

  • ImplantMax Software Ref K151152

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

Frequently asked questions

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

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

Which registries list Saturn Imaging, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Saturn Imaging, Inc. include ImplantMax Software.

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