510(k) Report

FDA applicant

41 Industries, LLC

Wheat Ridge, CO1 decision2008–20080 recalls

FDA records 1 decision for 41 Industries, LLC (Wheat Ridge, CO) in 2008: 1 510(k) clearance. All are in product code IQG (Adaptor, Holder, Syringe). 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 41 Industries, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2008

2008: 1
2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — 41 Industries, LLC by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • IQGAdaptor, Holder, Syringe1decision

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.

  • K072174Insucozi Insulin Vial Cover41 Industries, LLC · 20081cites it

What has FDA decided for it lately?

  • K072174Insucozi Insulin Vial Cover41 Industries, LLC · 2008

The one decision as 41 Industries, LLC →