FDA applicant

Xsirius Scientific, Inc.

Los Angeles, CA1 decision1986–19860 recalls

FDA records 1 decision for Xsirius Scientific, Inc. (Los Angeles, CA) in 1986: 1 510(k) clearance. All are in product code LIO (Device, Specimen Collection). 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, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Xsirius Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Xsirius Scientific, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Xsirius”

FDA records each applicant name separately; these may or may not be the same firm.

Xsirius Medical, Inc. 1

Xsirius Scientific, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Xsirius”