FDA applicant

The London Co.

Mchenry, IL7 decisions1976–19801 recall

FDA records 7 decisions for The London Co. (Mchenry, IL) from 1976 to 1980: 7 510(k) clearances. Most are in product codes CHL (Electrode Measurement, Blood-Gases (Pco2, Po2)…) and JFP (Electrode, Ion Specific, Calcium). 1 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, clinical chemistry panel, where it files most

How often FDA has decided The London Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The London Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The London Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “The”

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

London Diagnostics, Inc. 12 London Intl., LLC 6 London International Group, Inc. 5 London International U.S. Holdings, Inc. 2 London Rubber Co. (India), Ltd. 1

The London Co.

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?

What has been recalled?

Other applicant names beginning “The”