MDL MDL2513 (UDI D742MDL25130)Recalls & reported problems
Intra-Lock International, Inc. · MDL® ø2.5mm IMPLANT 13mm · Class 2 · Implant
All models of MDL (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 18
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI D742MDL25130), received between Feb 28, 2024 and Jan 24, 2025 — classified as 18 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (18 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 Osseointegrate18
Patient problems
- Insufficient Information18
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
InjuryJan 24, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 24, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 24, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 16, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 26, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 1, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 10, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 17, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 17, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 17, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 11, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 11, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 8, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
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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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