FDA applicant

Noah Medical Corp.

San Carlos, CA1 decision2023–20235 recalls

FDA records 1 decision for Noah Medical Corp. (San Carlos, CA) in 2023: 1 510(k) clearance. All are in product code EOQ (Bronchoscope (Flexible Or Rigid)). Its devices cite 1 predicate, 0 of them its own earlier devices. 5 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ear, nose and throat panel, where it files most

How often FDA has decided Noah Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2023high 1 (2023) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

1in 2025

2023high 4 (2024) · low 0 (2023)2026

Class I Class II/III not classified

FIG. 1 — Noah Medical Corp. by year, 2023–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Noah Medical Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

What has been recalled?