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A2z Radiology Ai, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
2

What A2z Radiology Ai, Inc. makes

A2z Radiology AI, Inc. develops a2z-Unified-Triage, a software-based triage tool designed to assist in prioritizing radiological imaging studies based on clinical urgency and workflow needs.

The company’s product portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The company is based in the US.

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

Catalogue2

Newest first, rows 1-2 of 2

  • a2z-Abdo-Triage Ref K260906

    Class II
    Active 510(k) 510(k) II
  • a2z-Unified-Triage Ref K252366

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does A2z Radiology Ai, Inc. have in the registry?

The registry currently lists 2 devices for A2z Radiology Ai, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list A2z Radiology Ai, Inc.'s devices?

Among its 2 most recently registered devices, A2z Radiology Ai, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do A2z Radiology Ai, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for A2z Radiology Ai, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from A2z Radiology Ai, Inc. in the registry?

The most recently registered devices listed for A2z Radiology Ai, Inc. include a2z-Abdo-Triage and a2z-Unified-Triage.

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