FDA applicant

Lexington Instruments

Mchenry, IL1 decision1977–19770 recalls

FDA records 1 decision for Lexington Instruments (Mchenry, IL) in 1977: 1 510(k) clearance. All are in product code DXG (Computer, Diagnostic, Pre-Programmed…). 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 Lexington Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lexington Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lexington”

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

Lexington Medical, Inc. 9 Lexington International, LLC 8 Lexington Industries 2

Lexington Instruments

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lexington”