510(k) Report

FDA applicant

Anc Import & Export Co., Ltd.

Arlington, TX1 decision2001–20010 recalls

FDA records 1 decision for Anc Import & Export Co., Ltd. (Arlington, TX) in 2001: 1 510(k) clearance. 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 Anc Import & Export Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anc Import & Export Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Anc Import & Export Co., Ltd. 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 Use1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K002910Holy Dragon Acupuncture NeedlesAnc Import & Export Co., Ltd. · 20011cites it

What has FDA decided for it lately?

  • K002910Holy Dragon Acupuncture NeedlesAnc Import & Export Co., Ltd. · 2001

The one decision as Anc Import & Export Co., Ltd. →