ALTATEC
Manufacturer adverse-event records for ALTATEC 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 · 2020–2026 · thin-book · quiet Death-code · injury-heavy
Volume signature
ALTATEC is a thinner MAUDE footprint
ALTATEC accounts for 3,736 FDA MAUDE reports (#434 of 434, thin-book tercile). Death-coded event_type share is 0.00% (quiet); Injury share 99.9% (injury-heavy).
What the volume reading shows for ALTATEC
The standout signal for ALTATEC is filing volume: 3,736 adverse-event reports in FDA MAUDE (#434 of 434, 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 1 device type, led in this extract by Injury at 3,733 (99.9% of event_type total). Peak single-year volume reaches 1,101 reports across 7 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 (1)
| Device | Reports |
|---|---|
| Implant, Endosseous, Root-Form | 3,736 |
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.