TRIVIDIA HEALTH, INC.
Manufacturer adverse-event records for TRIVIDIA HEALTH, INC. 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 · 2015–2026 · thin-book · quiet Death-code · injury-light
Injury-mix signature
TRIVIDIA HEALTH, INC. is lighter on Injury codes
Injury-coded event_type share is 0.3% (injury-light tercile) beside 0.03% Death-coded (quiet). Volume band: thin.
What the Injury-mix reading shows for TRIVIDIA HEALTH, INC.
The standout signal for TRIVIDIA HEALTH, INC. is Injury-mix: 0.3% Injury-coded (injury-light) beside 0.03% Death-coded, on a thin-book footprint.
As a thinner-book manufacturer, a handful of device families can swing the totals; open the device table rather than reading the company headline alone. Event_type counts are not the same population as Patient Outcomes.
Reports span 7 device types, led in this extract by Malfunction at 6,037 (99.6% of event_type total). Peak single-year volume reaches 2,117 reports across 12 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 (7)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.