Ditron Dental MPI-11420Recalls & reported problems
Ditron Dental Ltd · Molecular Precision Implant Ø4.20mm L11.5mm · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Ditron Dental MPI-11420 is a dental implant screw used to anchor a replacement tooth in the jawbone. The 58 reports describe the implant failing to fuse with the bone, sometimes losing that fusion after it had formed, and sometimes leading to infection around the site; all 58 involve injuries and none report a death. There are no recalls naming this device. Report activity was concentrated in the earlier 12-month period with 37 reports and none in the most recent 12 months.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 58
- Deaths reported
- 0
- Injuries reported
- 58
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 58 adverse event reports that list this exact device (DI 07290109280288), received between Jul 11, 2024 and Jul 30, 2025 — classified as 58 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (34 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate34
- Adverse Event Without Identified Device or Use Problem19
- Loss of Osseointegration5
Patient problems
- Inadequate Osseointegration39
- Unspecified Infection22
Recent adverse event reports
The 25 most recent of 58 reports, in the reporter's own words as published by the FDA.
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION. INFECTION.
Patient problems: Inadequate Osseointegration; Unspecified Infection
MAUDE report 22630894 ↗InjuryJul 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 28, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryFeb 5, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE. INFECTION.
Patient problems: Inadequate Osseointegration; Unspecified Infection
MAUDE report 21271597 ↗InjuryJan 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 22, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJan 9, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 9, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 9, 2025Failure to Osseointegrate; Failure to Osseointegrate
Other Implant, Endosseous, Root-Form devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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