FDA applicant

Aibiomed, Corp.

Santa Barbara, CA1 decision2018–20180 recalls

FDA records 1 decision for Aibiomed, Corp. (Santa Barbara, CA) in 2018: 1 De Novo grant. All are in product code QDF (Parathyroid Autofluorescence Detection Device). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2018

2018high 1 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Aibiomed, Corp. by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Aibiomed, Corp.

Which product codes does it file in?

What has FDA decided for it lately?