FDA applicant

Western Clinical Technology Systems, Inc.

San Antonio, TX1 decision2003–20030 recalls

FDA records 1 decision for Western Clinical Technology Systems, Inc. (San Antonio, TX) in 2003: 1 510(k) clearance. All are in product code IPF (Stimulator, Muscle, Powered). Its devices cite 1 predicate, 0 of them its own earlier devices. 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Western Clinical Technology Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Western Clinical Technology Systems, 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 Advanced Technology, Inc. 6 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 Clinical Technology Systems, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Western”