510(k) Report

FDA applicant

Genemax Medical Products Industry Corp.

Hsin Chu City, TW2 decisions2004–20040 recalls

FDA records 2 decisions for Genemax Medical Products Industry Corp. (Hsin Chu City, TW) in 2004: 2 510(k) clearances. All are in product code ITI (Wheelchair, Powered). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Genemax Medical Products Industry Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Genemax Medical Products Industry Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Genemax Medical Products Industry Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • ITIWheelchair, Powered2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K042749Genemax Power Wheelchair, PW4Genemax Medical Products Industry Corp. · 2004
  • K042748Genemax Power Wheelchair, PW3Genemax Medical Products Industry Corp. · 2004

All 2 as Genemax Medical Products Industry Corp. →