OKTAGON Dental Implant BLT RCRecalls & reported problems across all models
Hager & Meisinger Gesellschaft mit beschränkter Haftung · 6 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 43
- Deaths reported
- 0
- Injuries reported
- 41
- Recalls
- 0
We found 6 models of OKTAGON Dental Implant BLT RC by Hager & Meisinger Gesellschaft mit beschränkter Haftung in the FDA's device registry (GUDID). Together they are named in 43 adverse event reports in the FDA's MAUDE database, received between Apr 18, 2019 and Aug 5, 2022 — classified as 41 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (36 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
Most reported OKTAGON Dental Implant BLT RC problems
Device problems
- Failure to Osseointegrate36
- Unstable3
- Adverse Event Without Identified Device or Use Problem1
- Fracture1
- Inadequacy of Device Shape and/or Size1
- Therapeutic or Diagnostic Output Failure1
Patient problems
- Inadequate Osseointegration27
- No Clinical Signs, Symptoms or Conditions14
- Insufficient Information1
- Nerve Damage1
OKTAGON Dental Implant BLT RC models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- OKTAGON Dental Implant BLT RC 24002Implant, Endosseous, Root-Form15 reports
- OKTAGON Dental Implant BLT RC 24003Implant, Endosseous, Root-Form11 reports
- OKTAGON Dental Implant BLT RC 24001Implant, Endosseous, Root-Form6 reports
- OKTAGON Dental Implant BLT RC 24005Implant, Endosseous, Root-Form4 reports
- OKTAGON Dental Implant BLT RC 24006Implant, Endosseous, Root-Form4 reports
- OKTAGON Dental Implant BLT RC 24007Implant, Endosseous, Root-Form3 reports
Recent OKTAGON Dental Implant BLT RC adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 5, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION DUE TO INFECTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15173011 ↗InjuryJun 2, 2022Unstable
MISSING PRIMARYSTABILITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14572700 ↗InjuryJun 2, 2022Unstable
MISSING PRIMARY STABILITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14572699 ↗InjuryJun 2, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION, IMPLANT FALL OUT AFTER 3 WEEKS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14572697 ↗InjuryJun 2, 2022Unstable
MISSING PRIMARY STABILITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14572696 ↗InjuryMay 9, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14335219 ↗InjuryMay 9, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14335218 ↗InjuryApr 5, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING PRIMARY STABILITY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14013870 ↗InjuryMar 9, 2022Fracture; Fracture
BREAKAGE OF TRANSFER SCREW DUE TO HIGH TORQUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13712369 ↗InjuryMar 2, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 1, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 22, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION, POTENTIAL BIOMECHANICAL OVERLOAD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13575564 ↗
Other Hager & Meisinger Gesellschaft mit beschränkter Haftung products
All Hager & Meisinger Gesellschaft mit beschränkter Haftung 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 18, 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