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L.E.O. Corp.

Country not established

Devices
1

What L.E.O. Corp. makes

L.E.O. Corp. manufactures the LENS EASY ON, a device designed for ocular applications, likely intended for intraocular lens implantation or related procedures.

The LENS EASY ON is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) registry. The company 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

  • Lens Easy On Ref K822105

    Unclassified
    Active 510(k) 510(k) —

Frequently asked questions

How many devices does L.E.O. Corp. have in the registry?

The registry currently lists 1 device for L.E.O. Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list L.E.O. Corp.'s devices?

Among its 1 most recently registered device, L.E.O. Corp. has devices listed in FDA 510(k) (1 device).

What are the newest devices from L.E.O. Corp. in the registry?

The most recently registered devices listed for L.E.O. Corp. include LENS EASY ON.

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