Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005147469

FEI Number

3005147469

Entity Name

ADVANCED VISION TECHNOLOGIES

City/State/Country

Lakewood, CO, US

Establishment Address

969 S Kipling Pkwy, Lakewood, CO 80226, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ADVANCED VISION TECHNOLOGIES (Owner Number: 9071024)

Owner / Operator Contact Address

969 S. Kipling Pkwy, Lakewood, CO 80226, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K152724

PMA Number

N/A

All Registered Proprietary Names

Naturalens CRL NightLens EyePrintPro EPGP EyeFitPro ScanFitPro ScleraLens PediaSITE Naturalens Progressive Acuity Plus Transbylite CorneaLens PRIME Kone Naturalens VIP Cone PRIME Limbal SRG Naturalens MID PRO AVT Single Vision GP PRIME Limbal Naturalens GP Varifocal Plus NATURALENS MID PRO TRANSBYLITE DECARYLE BIFOCAL PRIME LIMBAL MCR EyePal Mini Scleral VIP CONE MCGUIRE CONE EyePrint Pro ScanFit Pro EyePal Scleral PRIME KONE Naturalens CRL CONCENTRIC BIFOCAL ACUITY NATURALENS MINI SCLERAL VARIFOCAL PLUS NATURALENS SCLERAL ACUITY PLUS AVT Scleral NATURALENS SOPER CONE PEDIASITE CorneaLens AVT Single Vision GP NATURALENS PROGRESSIVE EyePal Cone NightLens ScleraLens PK DESIGN HCR EyeFit Pro COMFORTLENS DRL EyeFitPRO EyePrintPRO ScanFitPRO Transbylite PRIME Kone Naturalens MID PRO Varifocal Plus ScleraLens PediaSITE AVT Single Vision GP CorneaLens Naturalens Progressive Acuity Plus PRIME Limbal SRG Naturalens GP Naturalens VIP Cone PRIME Limbal Continental 45 Sphere and Asphere (hefilcon A) Continental 45 Toric (hefilcon A) ScleraLens Eyeprint Pro Scleral GP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUU	Lens, Contact, Orthokeratology, Overnight	Ophthalmic	Class 3	886.5916	2023-12-14
MWL	Lens, Contact (Rigid Gas Permeable), Extended Wear	Ophthalmic	Class 3	886.5916	2023-12-14
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2021-02-15
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2022-06-08
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-06-08
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2022-06-08
LPL	Lenses, Soft Contact, Daily Wear	Ophthalmic	Class 2	886.5925	2018-12-21
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2021-12-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ADVANCED VISION TECHNOLOGIES

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
K133079	Alden Optical Labs., Inc.	IO2 SPHER(MANGOFILCON A) SOFT (HYDROPHILIC) CONTACT LENS FOR DAILY WEAR,IO2 TORIC (MANGOFILCON A) SOFT (HYDROPHILIC)	2013-12-17
K941998	Ocu-Ease Optical Products, Inc.	OCU-FLEX-38 (POLYMACON)	1994-10-13
K992500	Cantor & Silver , Ltd.	CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS	1999-08-18
K984098	Adventures IN Color Technology, Ltd.	ADVENTURE TINTS, COLOR ENHANCED TINTED SOFT CONTACT LENS	1999-05-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0018-07	Ciba Vision Corporation	2	CSI Daily Wear, soft (hydrophilic) contact lenses
Z-0019-07	Ciba Vision Corporation	2	CSI Flexible Wear, soft (hydrophilic) contact lenses
Z-0020-07	Ciba Vision Corporation	2	CSI Toric, soft (hydrophilic) contact lenses
Z-0044-2012	CooperVision Inc.	2	AVAIRA Toric (enfilcon A) TORIC soft (Hydrophilic) Contact Lenses, 6 SOFT CONTACT LENSES FOR ASTIGMATISM, CooperVision, Scottsville, NY 14546 USA; Juana Diaz, PR 00795 USA; Hamble SO31, 4RF, UK; Device Listing # D033736. Product Usage: Indicated for the correction of ametropia (myopia or hyperopia with astigmatism) in aphakic and non-aphakic persons with non-diseased eyes in powers from -20.00- to +20.00 diopters and astigmatic corrections from -0.25 to -10.00 diopters. The AVAIRA Soft Contact Lens is indicated for single - use disposable wear and daily wear. When prescribed for frequent replacement, the lens may be disinfected using a chemical or hydrogen peroxide disinfecting system.
Z-0326-2026	Alcon Research LLC	2	Alcon PRECISION1 One-Day Contact Lenses, -2.25D.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005147469. Last updated year: 2026. Please use registration number 3005147469 when referencing this establishment in official correspondence.