510(k) Report

FDA applicant

Freerider Corporation

Kang-Shan Dist, TW4 decisions2003–20170 recalls

FDA records 4 decisions for Freerider Corporation (Kang-Shan Dist, TW) from 2003 to 2017: 4 510(k) clearances. Most are in product codes ITI (Wheelchair, Powered) and INI (Vehicle, Motorized 3-Wheeled). Its devices cite 6 predicates, 2 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Freerider Corp”.

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 Freerider Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2017

2015: 22017: 1
2007high 2 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Freerider”

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