FDA applicant

Thomas M. Foti, M.D.

Mchenry, IL1 decision1982–19820 recalls

FDA records 1 decision for Thomas M. Foti, M.D. (Mchenry, IL) in 1982: 1 510(k) clearance. All are in product code ETF (Unit, Examining/Treatment, Ent). 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 Thomas M. Foti, M.D.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thomas M. Foti, M.D. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Thomas”

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

Thomas Medical Products, Inc. 23 Thomas Industries 9 Thomas J. Fogarty, M.D. 6 Thomas Medical, Inc. 2 Thomas G. Mason 1 Thomas Surgical Instruments, Inc. 1

Thomas M. Foti, M.D.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Thomas”