FDA applicant

Nuvon, Inc.

Washington, DC2 decisions2010–20130 recalls

FDA records 2 decisions for Nuvon, Inc. (Washington, DC) from 2010 to 2013: 2 510(k) clearances. All are in product code MWI (Monitor, Physiological, Patient (Without…). Its devices cite 3 predicates, 0 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, cardiovascular panel, where it files most

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

FDA decisions per year

1in 2013

2010high 1 (2010) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2010.

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

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Nuvon, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?