FDA applicant

Colorsoft Laboratories Corp.

Grand Junction, CO2 decisions1999–19990 recalls

FDA records 2 decisions for Colorsoft Laboratories Corp. (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 Colorsoft Laboratories Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Colorsoft Laboratories Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Colorsoft Laboratories Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Colorsoft Laboratories Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Colorsoft Laboratories Corp.

Which product codes does it file in?

What has FDA decided for it lately?