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Coagulating And Dissecting Electrode
No active recall
FDA product code: KNF · Category: Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)
Severity Snapshot
14 total reports2023-06 – 2025-12 date range92.9% physician / facility reported7.1% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
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Note: the 2018 Voluntary Malfunction Summary Reporting expansion means volume increases may reflect surveillance changes, not increased device risk.
Reported Events
Submitted to FDA MAUDE by physicians, hospitals, manufacturers, and patients.
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