FDA applicant

Tjn Manufacturing,Inc.

Davenport, IA2 decisions1992–19930 recalls

FDA records 2 decisions for Tjn Manufacturing,Inc. (Davenport, IA) from 1992 to 1993: 2 510(k) clearances. All are in product code JFB (Table, Physical Therapy, Multi Function). 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 Tjn Manufacturing,Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tjn Manufacturing,Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Tjn Manufacturing,Inc.

Which product codes does it file in?

What has FDA decided for it lately?