510(k) Report

FDA applicant

Golden Technologies, Inc.

Old Forge, PA8 decisions1988–20062 recalls

FDA records 8 decisions for Golden Technologies, Inc. (Old Forge, PA) from 1988 to 2006: 8 510(k) clearances. Most are in product codes INI (Vehicle, Motorized 3-Wheeled) and ITI (Wheelchair, Powered). Its devices cite 4 predicates, 3 of them its own earlier devices. 2 recalls are 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 Golden Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Golden Technologies, Inc. since 2007.

Recalls per year

1in 2020

2014: 12020: 1
2007high 1 (2014) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Golden”

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