Skip to content

Neo Optics, Inc.

Country not established

Devices
1

What Neo Optics, Inc. makes

Neo Optics, Inc. manufactures the KROM-X Lens System, a device designed for ocular applications, specifically intended for refractive correction through corneal reshaping.

The KROM-X Lens System 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, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Krom-X Lens System Ref K865103

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

Frequently asked questions

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

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

Which registries list Neo Optics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Neo Optics, Inc. include KROM-X LENS SYSTEM.

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