OKTAGON Dental Implant TL RP 72187Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · Tissue Level Implant Regular Platform Ø3,3x10 · Class 2 · Implant
All models of OKTAGON Dental Implant TL RP (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI E0HM721871), received between Apr 28, 2021 and Jul 22, 2022 — classified as 11 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (11 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 18, 2026.
Most reported problems
Device problems
- Failure to Osseointegrate11
- Fracture1
Patient problems
- Inadequate Osseointegration11
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
InjuryJul 22, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryJul 11, 2022Fracture; Failure to Osseointegrate; Fracture; Failure to Osseointegrate
InjuryApr 26, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 26, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 26, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 26, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 26, 2022Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 25, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION (INFECTION).
Patient problems: Inadequate Osseointegration
MAUDE report 14192123 ↗InjuryOct 22, 2021Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 22, 2021Failure to Osseointegrate; Failure to Osseointegrate
InjuryApr 28, 2021Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT WAS TO SMALL FOR THIS AREA, IMPLANT WASN'T PLACED.
Patient problems: Inadequate Osseointegration
MAUDE report 11736622 ↗
Other Implant, Endosseous, Root-Form devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
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 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