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MicroVention Web Sls
No active recall
Manufacturer: MicroVention · FDA product code: OPR · Category: Intrasaccular Flow Disruption Device
Severity Snapshot
45 total reports2020-11 – 2026-02 date range66.7% physician / facility reported33.3% 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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