infinity OCTAGON Bone Level Taper Dental ImplantRecalls & reported problems across all models
Hager & Meisinger Gesellschaft mit beschränkter Haftung · 10 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 95
- Deaths reported
- 0
- Injuries reported
- 95
- Recalls
- 0
We found 10 models of infinity OCTAGON Bone Level Taper Dental Implant by Hager & Meisinger Gesellschaft mit beschränkter Haftung in the FDA's device registry (GUDID). Together they are named in 95 adverse event reports in the FDA's MAUDE database, received between Feb 8, 2021 and Dec 11, 2024 — classified as 95 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (54 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 infinity OCTAGON Bone Level Taper Dental Implant problems
Device problems
- Failure to Osseointegrate54
- Patient Device Interaction Problem29
- Osseointegration Problem13
- Activation, Positioning or Separation Problem5
- Loss of Osseointegration4
- Inadequacy of Device Shape and/or Size1
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- Inadequate Osseointegration49
- Failure of Implant45
- Pain2
- Unspecified Infection1
infinity OCTAGON Bone Level Taper Dental Implant models
10 models, most reported first. Each model has its own page with its reports, recalls and device details.
- infinity OCTAGON Bone Level Taper Dental Implant BLT504110Implant, Endosseous, Root-Form28 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT504810Implant, Endosseous, Root-Form20 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT503310Implant, Endosseous, Root-Form10 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT504112Implant, Endosseous, Root-Form8 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT504808Implant, Endosseous, Root-Form7 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT503312Implant, Endosseous, Root-Form6 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT504108Implant, Endosseous, Root-Form6 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT503308Implant, Endosseous, Root-Form5 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT504812Implant, Endosseous, Root-Form3 reports
- infinity OCTAGON Bone Level Taper Dental Implant BLT503710Implant, Endosseous, Root-Form2 reports
Recent infinity OCTAGON Bone Level Taper Dental Implant adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryDec 11, 2024Loss of Osseointegration; Loss of Osseointegration
InjuryJun 14, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 12, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
MISSING OSSEOINTEGRATION AS TRANSFER PART BROKE DURING INSERTION.
Patient problems: Inadequate Osseointegration
MAUDE report 19099764 ↗InjuryApr 12, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
MISSING OSSEOINTEGRATION AS TRANSFER PART BROKE DURING INSERTION.
Patient problems: Inadequate Osseointegration
MAUDE report 19099691 ↗InjuryApr 12, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryApr 12, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 11, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 18, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 15, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryMar 15, 2024Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
InjuryMar 15, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryMar 5, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 13, 2024Loss of Osseointegration; Loss of Osseointegration
InjuryFeb 13, 2024Loss of Osseointegration; Loss of Osseointegration
InjuryDec 13, 2023Osseointegration Problem; Osseointegration Problem
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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