CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.4307Recalls & reported problems
ALTATEC GmbH · CONELOG® PROGRESSIVE-LINE Implant, Promote® plus, d 4.3 mm, L 7.0 mm · Class 2 · Implant
All models of CONELOG PROGRESSIVE-LINE Implant, Promote plus (36)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This CONELOG dental implant is designed to replace a tooth root. The 25 reports mostly describe the implant failing to bond with the jawbone, with limited details about the patient outcomes. There were 25 injuries and no deaths. No recalls name this device; reports fell from 14 in the previous 12 months to 8 in the latest 12 months.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 25
- Deaths reported
- 0
- Injuries reported
- 25
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI E219C108643071), received between Aug 5, 2024 and Jul 2, 2026 — classified as 25 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (21 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.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate21
- Use of Device Problem5
- Loss of Osseointegration1
Patient problems
- Insufficient Information25
Recent adverse event reports
The 25 most recent of 25 reports, in the reporter's own words as published by the FDA.
InjuryJul 2, 2026Failure to Osseointegrate
InjuryJun 9, 2026Failure to Osseointegrate
InjuryMay 4, 2026Failure to Osseointegrate
InjuryApr 21, 2026Failure to Osseointegrate
InjuryApr 21, 2026Failure to Osseointegrate
InjuryDec 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 10, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 15, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 14, 2025Use of Device Problem; Loss of Osseointegration; Use of Device Problem; Loss of Osseointegration
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 22806872 ↗InjuryJun 18, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 21, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryMay 16, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 22035305 ↗InjuryMay 16, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 22035198 ↗InjuryMay 1, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryFeb 5, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 21317903 ↗InjuryFeb 5, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryJan 22, 2025Use of Device Problem; Failure to Osseointegrate; Use of Device Problem; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryNov 27, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 25, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 17, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 5, 2024Failure to Osseointegrate; Failure to Osseointegrate
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.
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