Back to Microvention
MicroVention Web SL
No active recall
Manufacturer: MicroVention · FDA product code: OPR · Category: Intrasaccular Flow Disruption Device
Severity Snapshot
564 total reports2019-12 – 2026-03 date range90.1% physician / facility reported9.9% manufacturer reported1 SKU variants
Reporting Trend
Annual Reporting Volume
Click any bar to view those reports ↓
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.
Loading reports…