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Automated Imaging Diagnostics, LLC

Country not established

Devices
1

What Automated Imaging Diagnostics, LLC makes

Automated Imaging Diagnostics, LLC manufactures the neuropacs, a medical imaging system designed for diagnostic analysis of neurological structures, likely supporting applications such as neuroimaging and pathology assessment.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. The products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • neuropacs Ref DEN240071

    Active Regimes: De Novo Registry: De Novo Class:II

Frequently asked questions

How many devices does Automated Imaging Diagnostics, LLC have in the registry?

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

Which registries list Automated Imaging Diagnostics, LLC's devices?

Among its 1 most recently registered device, Automated Imaging Diagnostics, LLC has devices listed in FDA 510(k) (1 device).

What risk classes do Automated Imaging Diagnostics, LLC's devices fall under?

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

What are the newest devices from Automated Imaging Diagnostics, LLC in the registry?

The most recently registered devices listed for Automated Imaging Diagnostics, LLC include neuropacs.

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