FDA applicant

Louis M. Gerson Co., Inc.

Middleboro, MA8 decisions1980–20060 recalls

FDA records 8 decisions for Louis M. Gerson Co., Inc. (Middleboro, MA) from 1980 to 2006: 8 510(k) clearances. Most are in product codes FXX (Mask, Surgical) and MSH (Respirator, Surgical). Its devices cite 1 predicate, 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, general and plastic surgery panel, where it files most

How often FDA has decided Louis M. Gerson Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Louis M. Gerson Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Louis M. Gerson Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Louis”

FDA records each applicant name separately; these may or may not be the same firm.

Louis A. Serafin, Jr., M.D. 1

Louis M. Gerson Co., Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Louis”