Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022320387

FEI Number

3022320387

Entity Name

VALLEY CONTAX, INC

City/State/Country

Eugene, OR, US

Establishment Address

4748 Franklin Boulevard, Eugene, OR 97403, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Valley Contax (Owner Number: 10053951)

Owner / Operator Contact Address

4748 Franklin Boulevard, Eugene, OR 97403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Custom Stable Aurora Custom Stable GP scleral lens for daily wear Custom Stable Prime Custom Stable Elite Custom Stable Prime Gas Permeable Scleral Contact Lens Custom Stable Elite Gas Permeable Scleral Contact Lens Menicon Z rigid gas permeable contact lens Valley Lite APK Soper Valley Kone GP Scleral lens for Daily Wear KMax Edge Lift Comfort XL K Vault CAD Fixed ATS V Kone Platinumeye multifocal Custom Stable Pliaflex O2 I Kone GP Corneal lens for Daily Wear 11.2 Specialty CAD Hallmark multifocal Lasik Near Panafocal Goldeneye multifocal Valley Rev Geo Valley Kone 2 McGuire Prefix Multicurve Reverse Aspheric C.E.L.L

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-04-14
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-03-30
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2020-05-29

Official Correspondent

Robert Ahern

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Valley Contax

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
K963512	Benz Research and Development Corp.	BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL	1997-07-31

Similar Registrations

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3010607087	Menicon Nect Co., Ltd., Gujo Plant	Gujo Gifu, JP
1835957	ART OPTICAL CONTACT LENS, INC.	Walker, MI, US
3025308027	BIOLENS LAB	Mohammedia Mohammadia, MA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022320387. Last updated year: 2026. Please use registration number 3022320387 when referencing this establishment in official correspondence.