FDA applicant

Avicena, LLC

Altadena, CA2 decisions2019–20230 recalls

FDA records 2 decisions for Avicena, LLC (Altadena, CA) from 2019 to 2023: 2 510(k) clearances. Most are in product codes DQD (Stethoscope, Electronic) and QUO (Adjunctive Heart Failure Status Indicator). Its devices cite 2 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 Avicena, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2019high 1 (2019) · low 0 (2020)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2019.

FIG. 1 — Avicena, LLC by year, 2019–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Avicena, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?