510(k) Report

FDA applicant

Adventures IN Color Technology, Ltd.

Grand Junction, CO2 decisions1999–19990 recalls

FDA records 2 decisions for Adventures IN Color Technology, Ltd. (Grand Junction, CO) in 1999: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). 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 Adventures IN Color Technology, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Adventures IN Color Technology, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Adventures IN Color Technology, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LPLLenses, Soft Contact, Daily Wear2decisions

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K984098Adventure Tints, Color Enhanced Tinted Soft Contact LensAdventures IN Color Technology, Ltd. · 19991cites it

What has FDA decided for it lately?

  • K992054Adventure Tints Prosthetic Tinted Soft Contact LensAdventures IN Color Technology, Ltd. · 1999
  • K984098Adventure Tints, Color Enhanced Tinted Soft Contact LensAdventures IN Color Technology, Ltd. · 1999

All 2 as Adventures IN Color Technology, Ltd. →