510(k) Report

FDA applicant

Medox Corp.

Santa Ana, CA1 decision1995–19950 recalls

FDA records 1 decision for Medox Corp. (Santa Ana, CA) in 1995: 1 510(k) clearance. All are in product code CAF (Nebulizer (Direct Patient Interface)). 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 Medox Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medox Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medox Corp.’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)1decision

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.

  • K954327Medox Champion Compact NebulizerMedox Corp. · 19951cites it

What has FDA decided for it lately?

  • K954327Medox Champion Compact NebulizerMedox Corp. · 1995

The one decision as Medox Corp. →