FDA applicant

The Lagado Corp.

Chicago, IL5 decisions2004–20130 recalls

FDA records 5 decisions for The Lagado Corp. (Chicago, IL) from 2004 to 2013: 5 510(k) clearances. Most are in product codes HQD (Lens, Contact (Other Material) - Daily) and LRX (Case, Contact Lens). Its devices cite 4 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 The Lagado Corp.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2013

2007high 2 (2013) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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The Lagado Corp.

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?