FDA applicant

Martin'S Maine Exchange

Mchenry, IL4 decisions1980–19810 recalls

FDA records 4 decisions for Martin'S Maine Exchange (Mchenry, IL) from 1980 to 1981: 4 510(k) clearances. Most are in product codes NAD (Dressing, Wound, Occlusive) and DXQ (Blood Pressure Cuff). 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 hospital panel, where it files most

How often FDA has decided Martin'S Maine Exchange’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Martin'S Maine Exchange since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Martin'S Maine Exchange’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Martin'S”

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

Martin Medical 14 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 Electric Co. 1 Martin Pelvic Lift Co. 1

Martin'S Maine Exchange

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Martin'S”