FDA applicant

Martin Mclane Medical

La Mesa, CA1 decision1992–19920 recalls

FDA records 1 decision for Martin Mclane Medical (La Mesa, CA) in 1992: 1 510(k) clearance. All are in product code KDK (Container, Transport, Kidney). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Martin Mclane Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Martin Mclane 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 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 H. Kaufmann 1 Martin Electric Co. 1 Martin Pelvic Lift Co. 1

Martin Mclane Medical

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Martin”