FDA applicant

Martin Medical

Desoto, KS14 decisions1986–19870 recalls

FDA records 14 decisions for Martin Medical (Desoto, KS) from 1986 to 1987: 14 510(k) clearances. Most are in product codes LGF (Component, Cast) and LGH (Instrument, Cast Removal, Ac-Powered). 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Martin Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Martin Medical’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”

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

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 Electric Co. 1 Martin Pelvic Lift Co. 1

Martin Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Martin”