510(k) Report

FDA applicant

Pelican Products

Grnad Junction, CO1 decision2003–20030 recalls

FDA records 1 decision for Pelican Products (Grnad Junction, CO) in 2003: 1 510(k) clearance. All are in product code LRX (Case, Contact Lens). 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 Pelican Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pelican Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pelican Products 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?

  • LRXCase, Contact Lens1decision

Who builds on its devices?

Later devices cite its devices 3 times; 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.

  • K030987Contact Lens Storage CasePelican Products · 20033cite it

What has FDA decided for it lately?

  • K030987Contact Lens Storage CasePelican Products · 2003

The one decision as Pelican Products →

Other applicant names beginning “Pelican”

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

Pelican Bay Kel-Cor 1