Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043365583

FEI Number

3043365583

Entity Name

Visionary Optics, LLC

City/State/Country

Sterling, VA, US

Establishment Address

45472 Holiday Dr STE 5, Sterling, VA 20166, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Visionary Optics, LLC (Owner Number: 10031925)

Owner / Operator Contact Address

1325 Progress Drive, Front Royal, VA 22630, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Single Vision Latitude K-Max I-Kone XL-T Europa Scleral Elara Scleral Jupiter Scleral Reverse Geometry Europa Scleral Jupiter Scleral XL-T Latitude K-Max I-Kone Reverse Geometry Single Vision Elara Scleral XL-T Elara Scleral Jupiter Scleral Europa Scleral Latitude K-Max Reverse Geometry I-Kone Single Vision Europa Scleral, Jupiter Scleral, K-Max, Single Vision, Reverse Geometry, XL-T, I-Kone Elara Scleral Latitude Latitude Jupiter Scleral I-Kone Elara Scleral Reverse Geometry Single Vision K-Max Europa Scleral XL-T Europa Scleral, Jupiter Scleral, K-Max, Single Vision, Reverse Geometry, XL-T, I-Kone, Elara Scleral Latitude I-Kone Latitude K-Max Reverse Geometry XL-T Single Vision Jupiter Scleral Elara Scleral Europa Scleral Europa Scleral, Jupiter Scleral, K-Max, Single Vision, Reverse Geometry, XL-T, I-Kone, Elara Scleral Latitude Elara Scleral XL-T I-Kone Latitude Reverse Geometry K-Max Europa Scleral Single Vision Jupiter Scleral

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	2021-11-22
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2021-11-22
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-01-07
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2013-08-27
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2021-11-22
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2017-11-29
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2021-11-22
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2017-11-29
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2017-11-29
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2019-11-17
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2019-11-17

Official Correspondent

Sandra Freitez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Visionary Optics, LLC

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1000123221	Visionary Optics, LLC	Front Royal, VA, US

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

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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 3043365583. Last updated year: 2026. Please use registration number 3043365583 when referencing this establishment in official correspondence.