TORNIER S.A.S.
Manufacturer adverse-event records for TORNIER S.A.S. 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-heavy
Volume signature
TORNIER S.A.S. is a thinner MAUDE footprint
TORNIER S.A.S. accounts for 3,740 FDA MAUDE reports (#425 of 443, thin-book tercile). Death-coded event_type share is 0.00% (quiet); Injury share 93.8% (injury-heavy).
What the volume reading shows for TORNIER S.A.S.
The standout signal for TORNIER S.A.S. is filing volume: 3,740 adverse-event reports in FDA MAUDE (#425 of 443, thin-book). Death-coded event_type share sits at 0.00% (quiet).
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 20 device types, led in this extract by Injury at 3,507 (93.8% of event_type total). Peak single-year volume reaches 730 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 (20)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.