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Criss Optical Mfg. Co., Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1922662

Devices
1
Registrations
FDA
FDA recalls
0

What Criss Optical Mfg. Co., Inc. makes

CRISS Optical Manufacturing Co., Inc. produces the MAG-1 spectacle frame, a ready-to-wear eyeglass frame designed for general use.

The MAG-1 spectacle frame is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) database. 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

  • Mag-1 Spectacle Frame Ref K945342

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

Company details

FDA FEI number
1922662
Address
3628 S WEST ST, WICHITA, KS, 67217

Frequently asked questions

How many devices does CRISS OPTICAL MFG. CO., INC. have in the registry?

The registry currently lists 1 device for CRISS OPTICAL MFG. CO., INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list CRISS OPTICAL MFG. CO., INC.'s devices?

Among its 1 most recently registered device, CRISS OPTICAL MFG. CO., INC. has devices listed in FDA 510(k) (1 device).

What risk classes do CRISS OPTICAL MFG. CO., INC.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for CRISS OPTICAL MFG. CO., INC.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from CRISS OPTICAL MFG. CO., INC. in the registry?

The most recently registered devices listed for CRISS OPTICAL MFG. CO., INC. include MAG-1 SPECTACLE FRAME.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.