510(k) Report

FDA applicant

Equi-Tron Mfg., Inc.

Niagara Falls, NY5 decisions1989–19960 recalls

FDA records 5 decisions for Equi-Tron Mfg., Inc. (Niagara Falls, NY) from 1989 to 1996: 5 510(k) clearances. Most are in product codes FNL (Bed, Ac-Powered Adjustable Hospital) and GCX (Apparatus, Suction, Operating-Room, Wall…). 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 hospital panel, where it files most

How often FDA has decided Equi-Tron Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Equi-Tron Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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