JJGC S.A.
Manufacturer adverse-event records for JJGC S.A. 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 · heavy-book · quiet Death-code · injury-heavy
Death-code intensity
JJGC S.A. is quieter on Death-coded events
Death-coded event_type rows are 0 of 193,729 (0.00% · quiet tercile among 443 manufacturers). Absolute volume is heavy-book.
What the Death-code reading shows for JJGC S.A.
The standout signal for JJGC S.A. is Death-code intensity: 0.00% of 193,729 reports (quiet tercile), while absolute volume is heavy-book.
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair JJGC S.A. 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 4 device types, led in this extract by Injury at 193,729 (100.0% of event_type total). Peak single-year volume reaches 61,653 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 (4)
| Device | Reports |
|---|---|
| Implant, Endosseous, Root-Form | 193,687 |
| Implant, Endosseous, Orthodontic | 40 |
| Drill, Dental, Intraoral | 1 |
| Screwdriver, Surgical | 1 |
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.