FDA applicant

The LE Blanc Corp.

Augusta, GA2 decisions1989–19890 recalls

FDA records 2 decisions for The LE Blanc Corp. (Augusta, GA) in 1989: 2 510(k) clearances. All are in product code DSA (Cable, Transducer And Electrode, Patient…). 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, cardiovascular panel, where it files most

How often FDA has decided The LE Blanc Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The LE Blanc Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The LE Blanc Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?