CAMLOG SCREW-LINE Implant, Promote plusRecalls & reported problems across all models
ALTATEC GmbH · 60 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 628
- Deaths reported
- 0
- Injuries reported
- 628
- Recalls
- 0
We found 60 models of CAMLOG SCREW-LINE Implant, Promote plus by ALTATEC GmbH in the FDA's device registry (GUDID). Together they are named in 628 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2024 and Jul 12, 2026 — classified as 628 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (501 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 CAMLOG SCREW-LINE Implant, Promote plus problems
Device problems
- Failure to Osseointegrate501
- Use of Device Problem151
- Device Handling Problem6
- Fracture3
- Use of Incorrect Control/Treatment Settings2
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Insufficient Information628
CAMLOG SCREW-LINE Implant, Promote plus models
60 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3809Implant, Endosseous, Root-Form51 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.4309Implant, Endosseous, Root-Form41 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3811Implant, Endosseous, Root-Form38 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.5009Implant, Endosseous, Root-Form32 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.4311Implant, Endosseous, Root-Form31 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.3809Implant, Endosseous, Root-Form24 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.5011Implant, Endosseous, Root-Form21 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.3811Implant, Endosseous, Root-Form20 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.4309Implant, Endosseous, Root-Form20 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3813Implant, Endosseous, Root-Form20 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.6009Implant, Endosseous, Root-Form20 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.4311Implant, Endosseous, Root-Form17 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.5009Implant, Endosseous, Root-Form17 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.4311Implant, Endosseous, Root-Form15 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.4313Implant, Endosseous, Root-Form15 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.3311Implant, Endosseous, Root-Form14 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.6011Implant, Endosseous, Root-Form13 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.5011Implant, Endosseous, Root-Form12 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.3809Implant, Endosseous, Root-Form12 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.3811Implant, Endosseous, Root-Form12 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3311Implant, Endosseous, Root-Form12 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.4309Implant, Endosseous, Root-Form11 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.5011Implant, Endosseous, Root-Form11 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.3311Implant, Endosseous, Root-Form10 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.4313Implant, Endosseous, Root-Form10 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.4309Implant, Endosseous, Root-Form7 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.5011Implant, Endosseous, Root-Form7 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3313Implant, Endosseous, Root-Form7 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3816Implant, Endosseous, Root-Form7 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.4316Implant, Endosseous, Root-Form7 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3809Implant, Endosseous, Root-Form6 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.3813Implant, Endosseous, Root-Form6 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3811Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3813Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.5009Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.3313Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.4311Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.5013Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.3813Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.4313Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.4316Implant, Endosseous, Root-Form4 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.5013Implant, Endosseous, Root-Form4 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3313Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.3816Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.5009Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.6009Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.3313Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3311Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.4313Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.6009Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.4316Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.3816Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1055.5013Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3316Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.3816Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.4316Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® plus K1052.5013Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® plus K1054.6011Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.3316Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® plus K1056.6013Implant, Endosseous, Root-Form1 report
Recent CAMLOG 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 12, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJun 23, 2026Failure to Osseointegrate
InjuryJun 8, 2026Failure to Osseointegrate
InjuryJun 5, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 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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