DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)
Manufacturer adverse-event records for DENTSPLY IMPLANTS 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 · heavy-book · quiet Death-code · injury-heavy
Death-code intensity
DENTSPLY IMPLANTS is quieter on Death-coded events
Death-coded event_type rows are 0 of 84,605 (0.00% · quiet tercile among 434 manufacturers). Absolute volume is heavy-book.
What the Death-code reading shows for DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)
The standout signal for DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB) is Death-code intensity: 0.00% of 84,605 reports (quiet tercile), while absolute volume is heavy-book.
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair DENTSPLY IMPLANTS 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 6 device types, led in this extract by Injury at 82,660 (97.7% of event_type total). Peak single-year volume reaches 67,426 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 (6)
| Device | Reports |
|---|---|
| Implant, Endosseous, Root-Form | 82,563 |
| Accessories, Implant, Dental, Endosseous | 1,897 |
| Abutment, Implant, Dental, Endosseous | 142 |
| Bur, Dental | 1 |
| File, Pulp Canal, Endodontic | 1 |
| Instruments, Dental Hand | 1 |
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.