FDA applicant

Medicotest, Inc.

St. Louis, MO14 decisions1982–19990 recalls

FDA records 14 decisions for Medicotest, Inc. (St. Louis, MO) from 1982 to 1999: 14 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) and DRX (Electrode, Electrocardiograph). 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, neurology panel, where it files most

How often FDA has decided Medicotest, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medicotest, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Medicotest”

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

Medicotest A/S 7

Medicotest, Inc.

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?

Other applicant names beginning “Medicotest”