FDA applicant

Aeromax Technologies, Inc.

Phoenix, AZ1 decision1999–19990 recalls

FDA records 1 decision for Aeromax Technologies, Inc. (Phoenix, AZ) in 1999: 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 Aeromax Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Aeromax Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Aeromax Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?