ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER
Manufacturer adverse-event records for ALCON RESEARCH come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.
FDA MAUDE device safety record · 2015–2019 · mid-book · quiet Death-code · balanced
Death-code intensity
ALCON RESEARCH is quieter on Death-coded events
Death-coded event_type rows are 2 of 10,108 (0.02% · quiet tercile among 443 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER
The standout signal for ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER is Death-code intensity: 0.02% of 10,108 reports (quiet tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for ALCON RESEARCH. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 16 device types, led in this extract by Malfunction at 8,605 (85.1% of event_type total). Peak single-year volume reaches 2,703 reports across 5 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Devices (16)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.