Ditron Dental ULT-10420Recalls & reported problems
Ditron Dental Ltd · Ultimate Precision Implant Ø4.20mm L10mm · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Ditron Dental ULT-10420 is a narrow, short endosseous (root-form) dental implant. The 48 reports mostly describe the implant failing to fuse with the surrounding bone, or losing that bond after it had already formed, along with some infections. All 48 reports involve injuries, and none report a death. No recalls name this device. Reports fell sharply, from 26 in the previous 12 months to 3 in the most recent.
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
- 48
- Deaths reported
- 0
- Injuries reported
- 48
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 48 adverse event reports that list this exact device (DI 07290109280608), received between Apr 17, 2024 and Jun 23, 2026 — classified as 48 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (27 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 Osseointegrate27
- Loss of Osseointegration18
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Inadequate Osseointegration45
- Unspecified Infection3
Recent adverse event reports
The 25 most recent of 48 reports, in the reporter's own words as published by the FDA.
InjuryJun 23, 2026Failure to Osseointegrate
InjuryJun 21, 2026Failure to Osseointegrate
InjuryJun 21, 2026Failure to Osseointegrate
InjuryFeb 5, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryFeb 5, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 5, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 30, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 20, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 20, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 9, 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 2, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21052681 ↗InjuryJan 2, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 21052675 ↗InjuryDec 12, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 12, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20910847 ↗InjuryDec 12, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20910831 ↗InjuryDec 12, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20910789 ↗InjuryDec 12, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 5, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20850910 ↗InjuryDec 5, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20850898 ↗InjuryDec 5, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20850881 ↗InjuryDec 5, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20850872 ↗InjuryNov 28, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, INSTABILITY OF THE IMPLANT.
Patient problems: Inadequate Osseointegration
MAUDE report 20804139 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page