FDA applicant

Cbyon, Inc.

Palo Alto, CA2 decisions2000–20010 recalls

FDA records 2 decisions for Cbyon, Inc. (Palo Alto, CA) from 2000 to 2001: 2 510(k) clearances. All are in product code HAW (Neurological Stereotaxic Instrument). Its devices cite 1 predicate, 1 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Cbyon, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Cbyon, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?