510(k) Report

FDA applicant

Anco Merchandise Co., Ltd.

Taipei, Taiwan, R.O.C., CN1 decision1991–19910 recalls

FDA records 1 decision for Anco Merchandise Co., Ltd. (Taipei, Taiwan, R.O.C., CN) in 1991: 1 510(k) clearance. All are in product code JEQ (Toothbrush, Powered). 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, dental panel, where it files most

How often FDA has decided Anco Merchandise Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anco Merchandise Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Anco Merchandise Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Anco”

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