PlainHospital

NEODENT - JJGC S.A.

Manufacturer adverse-event records for NEODENT - 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 · 2017–2020 · heavy-book · quiet Death-code · injury-heavy

Injury-mix signature

NEODENT - JJGC S.A. leans injury-heavy in event_type mix

Injury-coded event_type share is 100.0% (injury-heavy tercile) beside 0.00% Death-coded (quiet). Volume band: heavy.

What the Injury-mix reading shows for NEODENT - JJGC S.A.

The standout signal for NEODENT - JJGC S.A. is Injury-mix: 100.0% Injury-coded (injury-heavy) beside 0.00% Death-coded, on a heavy-book footprint.

As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair NEODENT - 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 1 device type, led in this extract by Injury at 23,641 (100.0% of event_type total). Peak single-year volume reaches 7,715 reports across 4 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

23,646
Total Reports
1
Event-type Death
23,641
Injury Reports
1
Device Types

Event Types

Injury 23,641 (100.0%)
Malfunction 4 (0.0%)
Death 1 (0.0%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

Required Intervention 23,451 (99.2%)
188 (0.8%)
Other 6 (0.0%)
R 1 (0.0%)
Death 1 (0.0%)

Devices (1)

Device Reports
Implant, Endosseous, Root-Form 23,646

Yearly Trend

17
2017: 6,660
18
2018: 6,151
19
2019: 7,715
20
2020: 3,120

Read our methodology - how this data is sourced, computed, and verified.