MDLRecalls & reported problems across all models
Intra-Lock International, Inc. · 9 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 38
- Deaths reported
- 0
- Injuries reported
- 38
- Recalls
- 0
We found 9 models of MDL by Intra-Lock International, Inc. in the FDA's device registry (GUDID). Together they are named in 38 adverse event reports in the FDA's MAUDE database, received between Feb 16, 2024 and Apr 30, 2026 — classified as 38 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (37 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported MDL problems
Device problems
- Failure to Osseointegrate37
- Loss of Osseointegration2
- Fracture1
- Use of Device Problem1
Patient problems
- Insufficient Information38
MDL models
9 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MDL MDL2513Implant, Endosseous, Root-Form18 reports
- MDL MDL2513Implant, Endosseous, Root-Form8 reports
- MDL MDL2511Implant, Endosseous, Root-Form4 reports
- MDL MDL2513AImplant, Endosseous, Root-Form2 reports
- MDL MDL2513SImplant, Endosseous, Root-Form2 reports
- MDL MDL2510Implant, Endosseous, Root-Form1 report
- MDL MDL2511Implant, Endosseous, Root-Form1 report
- MDL MDL2515Implant, Endosseous, Root-Form1 report
- MDL MDL2515SImplant, Endosseous, Root-Form1 report
Recent MDL adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryApr 30, 2026Failure to Osseointegrate
InjuryFeb 12, 2026Failure to Osseointegrate
InjuryNov 4, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 23, 2025Failure to Osseointegrate; Failure to Osseointegrate
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 18, 2024Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 20250787 ↗InjurySep 18, 2024Failure to Osseointegrate; Failure to Osseointegrate
Other Intra-Lock International, Inc. products
All Intra-Lock International, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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