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Senomark Ultra Breast Tissue Marker
No active recall
FDA product code: NEU · Category: Marker, Radiographic, Implantable
Severity Snapshot
34 total reports2015-03 – 2026-02 date range52.9% physician / facility reported47.1% 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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