510(k) Report

FDA applicant

Goodman, Goodman & Goodman

Los Angelos, CA1 decision1998–19980 recalls

FDA records 1 decision for Goodman, Goodman & Goodman (Los Angelos, CA) in 1998: 1 510(k) clearance. 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 Goodman, Goodman & Goodman’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Goodman, Goodman & Goodman since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Goodman”

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