Data / Medical devices / United States / Advanced Vision Technologies

Advanced Vision Technologies: FDA-registered device maker in Lakewood, CO, United States, 6 510(k) clearances and 1 PMA approval

Name: Advanced Vision Technologies FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Advanced Vision Technologies is registered with the FDA (registration 3005147469) in Lakewood, CO, United States. It lists 5 device types. The FDA files 6 510(k) clearances and 1 PMA approval under its listings, the newest dated March 17, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3005147469
Address: 969 S Kipling Pkwy, Lakewood, CO, United States, 80226
Owner or operator: ADVANCED VISION TECHNOLOGIES (9071024)
Roles: Manufacturer
First device listed: January 16, 2013
Registered through: 2026
Brand names listed: ACUITY, ACUITY PLUS, AVT NaturaSOFT, AVT NaturaSOFT IC, AVT NaturaSOFT ICR, AVT NaturaSOFT Multi-Focal, AVT NaturaSOFT Toric, AVT Scleral and more

Devices it lists

Device	Product code	Class	Role	Source
Lens, Contact (Orthokeratology)	MUW	2	Manufacturer	accessdata.fda.gov
Lens, Contact (Other Material) - Daily	HQD	2	Manufacturer	accessdata.fda.gov
Lens, Contact (Rigid Gas Permeable), Extended Wear	MWL	3	Manufacturer	accessdata.fda.gov
Lens, Contact, Orthokeratology, Overnight	NUU	3	Manufacturer	accessdata.fda.gov
Lenses, Soft Contact, Daily Wear	LPL	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 17, 2022	K212631	Optimum Infinite (tisilfocon A) Daily Wear Contact Lenses	HQD	Substantially Equivalent	Contamac, Ltd.	accessdata.fda.gov
April 25, 2018	K180616	OPTIMUM GP (roflufocon D, roflurocon E) Daily Wear Contact Lens, HEXA100 (hexafocon A) Daily Wear Contact Lens	HQD	Substantially Equivalent	Contamac, Ltd.	accessdata.fda.gov
April 27, 2016	K152724	EYEPRINTPRO (ROFLUFOCON D) SCLERAL GP LENSES	HQD	Substantially Equivalent	Advanced Vision Technologies	accessdata.fda.gov
August 23, 2012	K121324	AVT NATURASOFT	LPL	Substantially Equivalent	Advanced Vision Technologies	accessdata.fda.gov
September 12, 2002	K021977	HYBRID FS & HYBRID FS TORIC (HYCOFOCON A) RGP CONTACT LENS FOR DAILY WEAR	HQD	Substantially Equivalent	Contamac, Ltd.	accessdata.fda.gov
May 11, 1999	K990011	CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR	LPL	Substantially Equivalent	Continental Soft Lens, Inc.	accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

Approved	PMA number	Device	Product code	Supplements	Latest decision	Source
June 7, 2004	P010062	EUCLID SYSTEMS ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENS FOR OVERNIGHT WEAR	NUU	14	December 16, 2025	accessdata.fda.gov

Compare with other makers

Updated December 16, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.