510(k) Report

FDA applicant

Maeda Toyokichi Shoten

Crofton, MD2 decisions2001–20020 recalls

FDA records 2 decisions for Maeda Toyokichi Shoten (Crofton, MD) from 2001 to 2002: 2 510(k) clearances. All are in product code MQX (Needle, Acupuncture, Single Use). 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, general hospital panel, where it files most

How often FDA has decided Maeda Toyokichi Shoten’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maeda Toyokichi Shoten since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Maeda Toyokichi Shoten 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?

  • MQXNeedle, Acupuncture, Single Use2decisions

What has FDA decided for it lately?

  • K021904Maeda Silver Acupuncture NeedleMaeda Toyokichi Shoten · 2002
  • K000581Maeda New Needle DisposableMaeda Toyokichi Shoten · 2001

All 2 as Maeda Toyokichi Shoten →