FDA applicant

The JM Kohn Co.

San Francisco, CA1 decision2002–20020 recalls

FDA records 1 decision for The JM Kohn Co. (San Francisco, CA) in 2002: 1 510(k) clearance. All are in product code NJB (Orthosis, Truncal, For Dysmenorrhea). 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, physical medicine panel, where it files most

How often FDA has decided The JM Kohn Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The JM Kohn Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The JM Kohn Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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The JM Kohn Co.

Which product codes does it file in?

What has FDA decided for it lately?