Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003701944

FEI Number

3003701944

Entity Name

OPTONOL, LTD

City/State/Country

NEVE ILAN Central, IL

Establishment Address

COMMUNICATION CENTER, NEVE ILAN Central 90850, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Alcon Laboratories, Inc. (Owner Number: 1610287)

Owner / Operator Contact Address

6201 South Freeway, Fort Worth, TX 76134, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K012852

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYF	Implant, Eye Valve	Ophthalmic	Class 2	886.3920	2010-03-02

Official Correspondent

No official correspondent registered.

US Agent Details

Dale Schaper Business: ALCON LABORATORIES, INC. Email: dale.schaper@alcon.com Phone: (817) 5686421

Related Public Records

Same Entity

Alcon Laboratories, Inc.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3013497605	Alcon Research, LLC	Sinking Spring, PA, US
3016232028	LUMITHERA, INC.	Fort Worth, TX, US
3006186389	CIBA VISION JOHOR SDN.BHD.,	GELANG PATAH, JOHOR DARUL TAKZIM, MY
3016075957	IVANTIS, INC.	Irvine, CA, US
1119421	Alcon Research, LLC	HUNTINGTON, WV, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003701944. Last updated year: 2026. Please use registration number 3003701944 when referencing this establishment in official correspondence.