OKTAGON Dental Implant BL RC 22005Recalls & reported problems
Hager & Meisinger Gesellschaft mit beschränkter Haftung · Bone Level Implant Regular Connect Ø4.8x8mm · Class 2 · Implant
All models of OKTAGON Dental Implant BL RC (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI E0HM220051), received between Apr 18, 2019 and Mar 31, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (4 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 Osseointegrate4
Patient problems
- Inadequate Osseointegration2
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMar 31, 2022Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION AND EXPLANTATION DUE TO PAIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13963224 ↗InjuryFeb 22, 2022Failure to Osseointegrate; Failure to Osseointegrate
FEHLENDE PRIMÄRSTABILITÄT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13575567 ↗InjuryJul 24, 2020Failure to Osseointegrate; Failure to Osseointegrate
MISSING OSSEOINTEGRATION AFTER 7 MONTH.
Patient problems: Inadequate Osseointegration
MAUDE report 10318491 ↗InjuryApr 18, 2019Failure to Osseointegrate; Failure to Osseointegrate
INADEQUATE PRIMARY STABILITY, HARD TIME REMOVING THE IMPLANT MOUNT.
Patient problems: Inadequate Osseointegration
MAUDE report 8526335 ↗
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
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- 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.
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