Skip to content

Eyesys Technologies, Inc.

Country not established

Devices
1

What Eyesys Technologies, Inc. makes

Eyesys Technologies, Inc. manufactures the EYE SYS VISTA, a device designed for ophthalmic imaging and diagnostic purposes, enabling detailed visualization of the retina and anterior segment of the eye.

The EYE SYS VISTA is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Eye Sys Vista Ref K973756

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

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

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

Which registries list Eyesys Technologies, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Eyesys Technologies, Inc. include EYE SYS VISTA.

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