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Cerenovus Enterprise
No active recall
FDA product code: NJE · Category: Intracranial Neurovascular Stent
Severity Snapshot
1,152 total reports2024-07 – 2026-03 date range99.6% physician / facility reported0.4% 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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