FDA applicant

Clark Davis Medical Systems, Inc.

London, Ontario, CA2 decisions1989–19910 recalls

FDA records 2 decisions for Clark Davis Medical Systems, Inc. (London, Ontario, CA) from 1989 to 1991: 2 510(k) clearances. Most are in product codes GWF (Stimulator, Electrical, Evoked Response) and GWE (Stimulator, Photic, Evoked Response). 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 Clark Davis Medical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clark Davis Medical Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Clark Davis Medical 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 “Clark”

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

Clark Laboratories, Inc. 14 Clark Research and Development, Inc. 2 Clark Pool & Assoc. 1 Clark Pillow Co., Inc. 1

Clark Davis Medical Systems, 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 “Clark”