Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1922662

FEI Number

1922662

Entity Name

CRISS OPTICAL MFG. CO., INC.

City/State/Country

WICHITA, KS, US

Establishment Address

3628 S WEST ST, WICHITA, KS 67217, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CRISS OPTICAL MFG. CO., INC. (Owner Number: 1216677)

Owner / Operator Contact Address

3628 SOUTH WEST ST., Wichita, KS 67217, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CRISSNYLON OPHTHAL CRISS NYLON OPHTHAL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	1995-02-27

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CRISS OPTICAL MFG. CO., INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1922662. Last updated year: 2026. Please use registration number 1922662 when referencing this establishment in official correspondence.