PlainHospital

ADIN DENTAL IMPLANT SYSTEMS LTD

Manufacturer adverse-event records for ADIN DENTAL IMPLANT SYSTEMS LTD 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 · 2022–2026 · mid-book · quiet Death-code · injury-heavy

Injury-mix signature

ADIN DENTAL IMPLANT SYSTEMS LTD 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: mid.

What the Injury-mix reading shows for ADIN DENTAL IMPLANT SYSTEMS LTD

The standout signal for ADIN DENTAL IMPLANT SYSTEMS LTD is Injury-mix: 100.0% Injury-coded (injury-heavy) beside 0.00% Death-coded, on a mid-book footprint.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for ADIN DENTAL IMPLANT SYSTEMS LTD. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 4 device types, led in this extract by Injury at 14,600 (100.0% of event_type total). Peak single-year volume reaches 7,398 reports across 5 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

14,602
Total Reports
0
Event-type Death
14,600
Injury Reports
4
Device Types

Event Types

Injury 14,600 (100.0%)
Malfunction 2 (0.0%)

Patient Outcomes

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

Required Intervention 14,568 (100.0%)

Devices (4)

Device Reports
Implant, Endosseous, Root-Form 14,572
Instruments, Dental Hand 17
Abutment, Implant, Dental, Endosseous 8
Accessories, Implant, Dental, Endosseous 5

Yearly Trend

22
2022: 3
23
2023: 41
24
2024: 1,813
25
2025: 5,347
26
2026: 7,398

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