CONELOG PROGRESSIVE-LINE Implant, Promote plusRecalls & reported problems across all models
ALTATEC GmbH · 36 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 977
- Deaths reported
- 0
- Injuries reported
- 977
- Recalls
- 0
We found 36 models of CONELOG PROGRESSIVE-LINE Implant, Promote plus by ALTATEC GmbH in the FDA's device registry (GUDID). Together they are named in 977 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2024 and Jul 12, 2026 — classified as 977 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (736 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 PROGRESSIVE-LINE Implant, Promote plus problems
Device problems
- Failure to Osseointegrate736
- Use of Device Problem264
- Osseointegration Problem3
- Connection Problem2
- Fracture2
- Loss of Osseointegration2
- Device Handling Problem1
- Expulsion1
Patient problems
- Insufficient Information977
CONELOG PROGRESSIVE-LINE Implant, Promote plus models
36 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.4309Implant, Endosseous, Root-Form103 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3811Implant, Endosseous, Root-Form99 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3809Implant, Endosseous, Root-Form78 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.4307Implant, Endosseous, Root-Form57 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.4311Implant, Endosseous, Root-Form55 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3311Implant, Endosseous, Root-Form45 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.5009Implant, Endosseous, Root-Form40 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3811Implant, Endosseous, Root-Form40 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.4309Implant, Endosseous, Root-Form37 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3813Implant, Endosseous, Root-Form32 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3309Implant, Endosseous, Root-Form29 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.4311Implant, Endosseous, Root-Form29 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.4313Implant, Endosseous, Root-Form27 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3313Implant, Endosseous, Root-Form26 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3311Implant, Endosseous, Root-Form26 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3807Implant, Endosseous, Root-Form25 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.4307Implant, Endosseous, Root-Form25 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.5007Implant, Endosseous, Root-Form21 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3809Implant, Endosseous, Root-Form21 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.5009Implant, Endosseous, Root-Form21 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3309Implant, Endosseous, Root-Form19 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.5011Implant, Endosseous, Root-Form18 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3313Implant, Endosseous, Root-Form15 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3813Implant, Endosseous, Root-Form15 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.4313Implant, Endosseous, Root-Form14 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.5007Implant, Endosseous, Root-Form14 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3807Implant, Endosseous, Root-Form10 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.5011Implant, Endosseous, Root-Form10 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3816Implant, Endosseous, Root-Form9 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.5013Implant, Endosseous, Root-Form5 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3316Implant, Endosseous, Root-Form3 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.3816Implant, Endosseous, Root-Form3 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.3316Implant, Endosseous, Root-Form2 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.5013Implant, Endosseous, Root-Form2 reports
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1085.4316Implant, Endosseous, Root-Form1 report
- CONELOG® PROGRESSIVE-LINE Implant, Promote® plus C1086.4316Implant, Endosseous, Root-Form1 report
Recent CONELOG PROGRESSIVE-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 12, 2026Failure to Osseointegrate
InjuryJul 12, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJul 6, 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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