Ditron Dental MPI-10375Recalls & reported problems
Ditron Dental Ltd · Molecular Precision Implant Ø3.75mm L10.0mm · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Ditron Dental Molecular Precision implant is a small dental implant placed in the jawbone to support a replacement tooth. Its 142 reports mostly describe implants that failed to bond with the bone or lost that bond, and some mention infection. There are no deaths and 142 injuries. No recalls name this device. Reports fell to 3 in the last 12 months from 92 before.
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
- 142
- Deaths reported
- 0
- Injuries reported
- 142
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 142 adverse event reports that list this exact device (DI 07290109280219), received between Apr 17, 2024 and Jun 23, 2026 — classified as 142 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (81 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 Osseointegrate81
- Adverse Event Without Identified Device or Use Problem35
- Loss of Osseointegration27
Patient problems
- Inadequate Osseointegration107
- Unspecified Infection37
Recent adverse event reports
The 25 most recent of 142 reports, in the reporter's own words as published by the FDA.
InjuryJun 23, 2026Loss of Osseointegration
InjuryJun 21, 2026Failure to Osseointegrate
InjuryJun 21, 2026Failure to Osseointegrate; Loss of Osseointegration
FAILURE TO OSSEOINTEGRATE. LOSS OF OSSEOINTEGRATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25571813 ↗InjurySep 15, 2025Loss of Osseointegration; Loss of Osseointegration
InjurySep 15, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 30, 2025Loss of Osseointegration; Loss of Osseointegration
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, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 30, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
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, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 29, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJul 29, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 29, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryJul 29, 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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