Ditron Dental ULT-11420Recalls & reported problems
Ditron Dental Ltd · Ultimate 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 Ultimate Precision dental implant has 25 adverse event reports, all involving injuries and no deaths. The reports mostly describe the implant failing to fuse with the jawbone or losing that bond later, leaving the implant unstable. 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
- 25
- Deaths reported
- 0
- Injuries reported
- 25
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 07290109280646), received between Jul 14, 2024 and Jan 30, 2025 — classified as 25 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (16 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 Osseointegrate16
- Loss of Osseointegration8
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Inadequate Osseointegration24
- Unspecified Infection1
Recent adverse event reports
The 25 most recent of 25 reports, in the reporter's own words as published by the FDA.
InjuryJan 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 9, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21108986 ↗InjuryJan 9, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21108984 ↗InjuryJan 2, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21052688 ↗InjuryJan 2, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21052676 ↗InjuryJan 2, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21052647 ↗InjuryDec 12, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 12, 2024Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE, THE IMPLANT FELL DOWN.
Patient problems: Inadequate Osseointegration
MAUDE report 20910797 ↗InjuryDec 5, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE, THE IMPLANT FELL DOWN.
Patient problems: Inadequate Osseointegration
MAUDE report 20804138 ↗InjuryNov 28, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20804089 ↗InjuryNov 21, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryNov 21, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 21, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20742953 ↗InjuryNov 21, 2024Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE, THE IMPLANT FELL DOWN.
Patient problems: Inadequate Osseointegration
MAUDE report 20742912 ↗InjuryOct 13, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 6, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20379676 ↗InjurySep 29, 2024Failure to Osseointegrate; Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE, THE IMPLANT FELL DOWN.
Patient problems: Inadequate Osseointegration
MAUDE report 20329951 ↗InjuryAug 8, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 18, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 14, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 14, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 14, 2024Failure to Osseointegrate; Failure to Osseointegrate
Other Implant, Endosseous, Root-Form devices
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- 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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