MENTOR TEXAS
Manufacturer adverse-event records for MENTOR TEXAS 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 · 1998–2026 · heavy-book · quiet Death-code · injury-heavy
Death-code intensity
MENTOR TEXAS is quieter on Death-coded events
Death-coded event_type rows are 0 of 111,158 (0.00% · quiet tercile among 443 manufacturers). Absolute volume is heavy-book.
What the Death-code reading shows for MENTOR TEXAS
The standout signal for MENTOR TEXAS is Death-code intensity: 0.00% of 111,158 reports (quiet tercile), while absolute volume is heavy-book.
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair MENTOR TEXAS with device-family pages before treating company totals as a safety verdict. Event_type Death and Injury are one code per report; Patient Outcomes below use a separate FDA population.
Reports span 12 device types, led in this extract by Injury at 109,189 (98.2% of event_type total). Peak single-year volume reaches 15,412 reports across 16 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 (12)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.