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Manta
No active recall
FDA product code: MGB · Category: Device, Hemostasis, Vascular
Severity Snapshot
1,441 total reports2019-11 – 2026-03 date range44.2% physician / facility reported55.8% manufacturer reported21 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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