FDA applicant

Wet Nose Technologies, LLC

Los Angeles, CA2 decisions2010–20110 recalls

FDA records 2 decisions for Wet Nose Technologies, LLC (Los Angeles, CA) from 2010 to 2011: 2 510(k) clearances. All are in product code CBP (Valve, Non-Rebreathing). Its devices cite 2 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 Wet Nose Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2010high 1 (2010) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

FIG. 1 — Wet Nose Technologies, LLC by year, 2010–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Wet Nose Technologies, LLC

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?