510(k) Report

FDA applicant

Intl. Medical Marketing, Inc.

Ridge, NY5 decisions1989–19900 recalls

FDA records 5 decisions for Intl. Medical Marketing, Inc. (Ridge, NY) from 1989 to 1990: 5 510(k) clearances. Most are in product codes FPD (Tube, Feeding) and KNX (Collector, Urine, (And Accessories) For…). 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 Intl. Medical Marketing, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Intl. Medical Marketing, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Intl. Medical Marketing, Inc.’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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