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OKTAGON Dental Implant TL RPRecalls & reported problems across all models

Hager & Meisinger Gesellschaft mit beschränkter Haftung · 7 models in the FDA device registry

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
24
Deaths reported
0
Injuries reported
24
Recalls
0

We found 7 models of OKTAGON Dental Implant TL RP by Hager & Meisinger Gesellschaft mit beschränkter Haftung in the FDA's device registry (GUDID). Together they are named in 24 adverse event reports in the FDA's MAUDE database, received between Dec 2, 2020 and May 26, 2023 — classified as 24 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (24 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 TL RP problems

Device problems

  • Failure to Osseointegrate24
  • Fracture2
  • Loss of Osseointegration1
  • Osseointegration Problem1
  • Patient Device Interaction Problem1

Patient problems

  • Inadequate Osseointegration23
  • Failure of Implant1

OKTAGON Dental Implant TL RP models

7 models, most reported first. Each model has its own page with its reports, recalls and device details.

Recent OKTAGON Dental Implant TL RP adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

Other Hager & Meisinger Gesellschaft mit beschränkter Haftung products

All Hager & Meisinger Gesellschaft mit beschränkter Haftung devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page