510(k) Report

FDA applicant

Advanced Vision Technologies

Lakewood, CO2 decisions2012–20160 recalls

FDA records 2 decisions for Advanced Vision Technologies (Lakewood, CO) from 2012 to 2016: 2 510(k) clearances. Most are in product codes HQD (Lens, Contact (Other Material) - Daily) and LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 5 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Advanced Vision Technologies’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2012: 12016: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Advanced Vision Technologies by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • HQDLens, Contact (Other Material) - Daily1decision
  • LPLLenses, Soft Contact, Daily Wear1decision

Whose devices does it build on?

Its devices cite 5 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K152724Eyeprintpro (Roflufocon D) Scleral GP LensesAdvanced Vision Technologies · 2016
  • K121324Avt NaturasoftAdvanced Vision Technologies · 2012

All 2 as Advanced Vision Technologies →