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Artann Laboratories, Inc.

Country not established

Devices
1

What Artann Laboratories, Inc. makes

Artann Laboratories, Inc. manufactures a prostate mechanical imager, a device designed for imaging and diagnostic purposes in prostate health assessments.

The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Prostate Mechanical Imager Ref DEN100016

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

Frequently asked questions

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

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

Which registries list Artann Laboratories, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Artann Laboratories, Inc. include PROSTATE MECHANICAL IMAGER.

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