FDA applicant

Les Laboratoires Blanchard

Chicago, IL2 decisions1998–20000 recalls

FDA records 2 decisions for Les Laboratoires Blanchard (Chicago, IL) from 1998 to 2000: 2 510(k) clearances. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 2 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 Les Laboratoires Blanchard’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Les Laboratoires Blanchard since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Les Laboratoires Blanchard

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?