FDA applicant

Martin D. Lerman

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Martin D. Lerman (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code KMY (Positioner, Tooth, Preformed). 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, dental panel, where it files most

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

FDA decisions per year

No FDA decision for Martin D. Lerman since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Martin D. Lerman 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 Manufacturing Co., LLC 1 Martin Mclane Medical 1 Martin H. Kaufmann 1 Martin Electric Co. 1 Martin Pelvic Lift Co. 1

Martin D. Lerman

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Martin”