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Xenform
No active recall
FDA product code: FTM · Category: Mesh, Surgical
Severity Snapshot
767 total reports2009-07 – 2025-05 date range0.1% physician / facility reported99.9% 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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