FDA applicant

Westcon Contact Lens Co., Inc.

Grnad Junction, CO11 decisions1994–20080 recalls

FDA records 11 decisions for Westcon Contact Lens Co., Inc. (Grnad Junction, CO) from 1994 to 2008: 10 510(k) clearances and 1 original PMA approval. Most are in product codes LPL (Lenses, Soft Contact, Daily Wear) and LPM (Lenses, Soft Contact, Extended Wear). Its devices cite 7 predicates, 6 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Westcon Contact Lens Co.”.

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 Westcon Contact Lens Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Westcon Contact Lens Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Westcon Contact Lens Co., Inc.’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

Other applicant names beginning “Westcon”

FDA records each applicant name separately; these may or may not be the same firm.

Westcon Orthopedics, Inc. 4

Westcon Contact Lens Co., Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Westcon”