510(k) Report

FDA applicant

Acusupply, Inc.

Aventura, FL3 decisions2001–20010 recalls

FDA records 3 decisions for Acusupply, Inc. (Aventura, FL) in 2001: 3 510(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 Acusupply, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Acusupply, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Acusupply, Inc. 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 Use3decisions

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.

  • K011247Holy Dragon Sterile Acupuncture Needle for Single UseAcusupply, Inc. · 20011cites it

What has FDA decided for it lately?

  • K011248CW Disposable Acupuncture NeedleAcusupply, Inc. · 2001
  • K011247Holy Dragon Sterile Acupuncture Needle for Single UseAcusupply, Inc. · 2001
  • K011242Huanqiu and Super (Two Brands) Sterile Acupuncture Needle for Single UseAcusupply, Inc. · 2001

All 3 as Acusupply, Inc. →