510(k) Report

FDA applicant

Cybernius Medical, Ltd.

St. Albert, Alberta, CA1 decision1997–19970 recalls

FDA records 1 decision for Cybernius Medical, Ltd. (St. Albert, Alberta, CA) in 1997: 1 510(k) clearance. All are in product code KPF (System, Dialysate Delivery, Semi-Automatic…). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Cybernius Medical, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • KPFSystem, Dialysate Delivery, Semi-Automatic, Peritoneal1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K970989CyberrenCybernius Medical, Ltd. · 19971cites it

What has FDA decided for it lately?

  • K970989CyberrenCybernius Medical, Ltd. · 1997

The one decision as Cybernius Medical, Ltd. →