510(k) Report

FDA applicant

Mar-Med Co.

Grand Rapids, MI1 decision1993–19930 recalls

FDA records 1 decision for Mar-Med Co. (Grand Rapids, MI) in 1993: 1 510(k) clearance. All are in product code GDJ (Clamp, Surgical, General & Plastic Surgery). 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 Mar-Med Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mar-Med Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • GDJClamp, Surgical, General & Plastic Surgery1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K924223Mar-Med Liver StrapMar-Med Co. · 19931cites it

What has FDA decided for it lately?

  • K924223Mar-Med Liver StrapMar-Med Co. · 1993

The one decision as Mar-Med Co. →