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Ai Optics

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Devices
1

What Ai Optics makes

Ai Optics manufactures the Sentinel Camera, a medical imaging device designed for real-time monitoring and documentation in clinical settings.

The Sentinel Camera is classified as a Class II 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Sentinel Camera Ref K243664

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

Frequently asked questions

How many devices does Ai Optics have in the registry?

The registry currently lists 1 device for Ai Optics. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ai Optics's devices?

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

What risk classes do Ai Optics's devices fall under?

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

What are the newest devices from Ai Optics in the registry?

The most recently registered devices listed for Ai Optics include Sentinel Camera.

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