510(k) Report

FDA applicant

Multigon Industries, Inc.

Mt. Vernon, NY8 decisions1985–20050 recalls

FDA records 8 decisions for Multigon Industries, Inc. (Mt. Vernon, NY) from 1985 to 2005: 8 510(k) clearances. Most are in product codes IYN (System, Imaging, Pulsed Doppler, Ultrasonic) and DPT (Probe, Blood-Flow, Extravascular). Its devices cite 9 predicates, 1 of them its own earlier devices. 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Multigon Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multigon Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Multigon Industries, 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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