510(k) Report

FDA applicant

E. Benson Hood Laboratories, Inc.

Mchenry, IL6 decisions1984–19990 recalls

FDA records 6 decisions for E. Benson Hood Laboratories, Inc. (Mchenry, IL) from 1984 to 1999: 6 510(k) clearances. Most are in product codes BTO (Tube, Tracheostomy (W/Wo Connector)) and FWN (Prosthesis, Larynx (Stents And Keels)). 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, ear, nose and throat panel, where it files most

How often FDA has decided E. Benson Hood Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for E. Benson Hood Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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