Ditron Dental MPI-13375Recalls & reported problems
Ditron Dental Ltd · Molecular Precision Implant Ø3.75mm L13mm · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Ditron Dental MPI-13375 is a small screw-shaped dental implant placed in the jawbone to replace a missing tooth. The 50 reports mostly describe the implant failing to fuse with the surrounding bone, or that fusion being lost later, along with some infections. All 50 reports involve injuries, and no deaths are mentioned. No recalls name this device.
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
- 50
- Deaths reported
- 0
- Injuries reported
- 50
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 50 adverse event reports that list this exact device (DI 07290109280332), received between Apr 17, 2024 and Jun 23, 2026 — classified as 50 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (29 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate29
- Loss of Osseointegration14
- Adverse Event Without Identified Device or Use Problem7
Patient problems
- Inadequate Osseointegration42
- Unspecified Infection7
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 25 most recent of 50 reports, in the reporter's own words as published by the FDA.
InjuryJun 23, 2026Loss of Osseointegration
InjuryJun 22, 2026Loss of Osseointegration
InjuryJun 21, 2026Failure to Osseointegrate
InjuryJun 21, 2026Failure to Osseointegrate
InjuryJun 21, 2026Failure to Osseointegrate
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 29, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 28, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 22, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 22, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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