CONELOG SCREW-LINE Implant, Promote plusRecalls & reported problems across all models
ALTATEC GmbH · 44 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 194
- Deaths reported
- 0
- Injuries reported
- 194
- Recalls
- 0
We found 44 models of CONELOG SCREW-LINE Implant, Promote plus by ALTATEC GmbH in the FDA's device registry (GUDID). Together they are named in 194 adverse event reports in the FDA's MAUDE database, received between Feb 27, 2024 and Jul 8, 2026 — classified as 194 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (158 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 CONELOG SCREW-LINE Implant, Promote plus problems
Device problems
- Failure to Osseointegrate158
- Use of Device Problem45
- Osseointegration Problem1
Patient problems
- Insufficient Information194
CONELOG SCREW-LINE Implant, Promote plus models
44 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.3809Implant, Endosseous, Root-Form20 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3309Implant, Endosseous, Root-Form16 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.3807Implant, Endosseous, Root-Form14 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.3309Implant, Endosseous, Root-Form10 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.3811Implant, Endosseous, Root-Form10 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.4309Implant, Endosseous, Root-Form10 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.4307Implant, Endosseous, Root-Form8 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.4307Implant, Endosseous, Root-Form8 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.5007Implant, Endosseous, Root-Form8 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.5007Implant, Endosseous, Root-Form7 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3809Implant, Endosseous, Root-Form7 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3811Implant, Endosseous, Root-Form7 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3807Implant, Endosseous, Root-Form5 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3807Implant, Endosseous, Root-Form5 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3313Implant, Endosseous, Root-Form4 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.4311Implant, Endosseous, Root-Form4 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3813Implant, Endosseous, Root-Form4 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3309Implant, Endosseous, Root-Form3 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.4311Implant, Endosseous, Root-Form3 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.3311Implant, Endosseous, Root-Form3 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.4309Implant, Endosseous, Root-Form3 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.3811Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.4311Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.5007Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.5011Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3311Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3809Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3811Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.4309Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.4313Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.5009Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3311Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.4311Implant, Endosseous, Root-Form2 reports
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.3813Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.4309Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.3813Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.4307Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1064.5007Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.3813Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1065.5011Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.3313Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.4316Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1066.5009Implant, Endosseous, Root-Form1 report
- CONELOG® SCREW-LINE Implant, Promote® plus C1062.3311Implant, Endosseous, Root-Form1 report
Recent CONELOG SCREW-LINE Implant, Promote plus adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJun 18, 2026Failure to Osseointegrate
InjuryJun 16, 2026Failure to Osseointegrate
InjuryJun 10, 2026Failure to Osseointegrate
InjuryJun 5, 2026Failure to Osseointegrate
InjuryJun 5, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25382940 ↗InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryMay 26, 2026Failure to Osseointegrate
InjuryMay 20, 2026Failure to Osseointegrate
InjuryMay 20, 2026Failure to Osseointegrate
InjuryMay 20, 2026Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25233942 ↗InjuryMay 14, 2026Failure to Osseointegrate
Other ALTATEC GmbH products
All ALTATEC GmbH 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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