510(k) Report

FDA applicant

Nexus6, Ltd.

Auckland, NZ2 decisions2009–20140 recalls

FDA records 2 decisions for Nexus6, Ltd. (Auckland, NZ) from 2009 to 2014: 2 510(k) clearances. All are in product code CAF (Nebulizer (Direct Patient Interface)). Its devices cite 4 predicates, 1 of them its own earlier devices. 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, anesthesiology panel, where it files most

How often FDA has decided Nexus6, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2009: 12014: 1
2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Nexus6, Ltd. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nexus6, 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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Which product codes does it file in?

  • CAFNebulizer (Direct Patient Interface)2decisions

Whose devices does it build on?

Its devices cite 4 predicates; 1 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 times; 1 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.

  • K091803Smarttrack SystemNexus6, Ltd. · 20092cite it
  • K133951SmarttouchNexus6, Ltd. · 20142cite it

What has FDA decided for it lately?

  • K133951SmarttouchNexus6, Ltd. · 2014
  • K091803Smarttrack SystemNexus6, Ltd. · 2009

All 2 as Nexus6, Ltd. →