FDA applicant

Western Advanced Technology, Inc.

Mchenry, IL6 decisions1980–19830 recalls

FDA records 6 decisions for Western Advanced Technology, Inc. (Mchenry, IL) from 1980 to 1983: 6 510(k) clearances. Most are in product codes ETS (Generator, Electronic Noise (For Audiometric…) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Western Advanced Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Western Advanced Technology, 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 “Western”

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

Western Laboratories Corp. 7 Western Medical, Ltd. 4 Western Medical Products, Inc. 3 Western Systems Research, Inc. 2 Western M/D, Inc. 2 Western Surgical Instrument Co. 1 Western Medical Equipment Corp. 1 Western/Scott Fetzer Co. 1 Western Systems, Inc. 1 The Western Diagnostics Co. 1 Western Medical Research 1 Western Dialysis Supplies, Ltd. 1

Western Advanced Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Western”