FDA applicant

Slenderizers Equipment Mfg., Inc.

Arnold, MO7 decisions1987–19880 recalls

FDA records 7 decisions for Slenderizers Equipment Mfg., Inc. (Arnold, MO) from 1987 to 1988: 7 510(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 Slenderizers Equipment Mfg., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Slenderizers Equipment Mfg., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Slenderizers Equipment Mfg., Inc.

Which product codes does it file in?

What has FDA decided for it lately?