FDA applicant

Martin Electric Co.

Walker, MI1 decision1979–19790 recalls

FDA records 1 decision for Martin Electric Co. (Walker, MI) in 1979: 1 510(k) clearance. All are in product code KCX (Epilator, High Frequency, Tweezer-Type). 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, general and plastic surgery panel, where it files most

How often FDA has decided Martin Electric Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Martin Electric Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Martin Electric Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Martin”

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

Martin Medical 14 Martin'S Maine Exchange 4 Martin Uram, MD 2 Martin S. Knopf Assoc., Inc. 2 Martin Dalsing 2 Martin E. Wendelken 1 Martin A. Hass, D.D.S. 1 Martin D. Lerman 1 Martin Manufacturing Co., LLC 1 Martin Mclane Medical 1 Martin H. Kaufmann 1 Martin Pelvic Lift Co. 1

Martin Electric Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Martin”