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Deeplook, Inc.

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Devices
1

What Deeplook, Inc. makes

Deeplook, Inc. manufactures the DeepLook PRECISE, a medical imaging device designed for retinal imaging and analysis, enabling detailed visualization of the eye’s interior structures.

The DeepLook PRECISE 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

  • DeepLook PRECISE Ref K202084

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

Frequently asked questions

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

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

Which registries list Deeplook, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Deeplook, Inc. include DeepLook PRECISE.

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