510(k) Report

FDA applicant

Micromedical Technologies, Inc.

Chatham, IL5 decisions1987–19970 recalls

FDA records 5 decisions for Micromedical Technologies, Inc. (Chatham, IL) from 1987 to 1997: 5 510(k) clearances. Most are in product codes GWN (Nystagmograph) and LXV (Apparatus, Vestibular Analysis). 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 Micromedical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micromedical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micromedical Technologies, 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 “Micromedical”

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