CAMLOG SCREW-LINE Implant, PromoteRecalls & reported problems across all models
ALTATEC GmbH · 30 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 80
- Deaths reported
- 0
- Injuries reported
- 80
- Recalls
- 0
We found 30 models of CAMLOG SCREW-LINE Implant, Promote by ALTATEC GmbH in the FDA's device registry (GUDID). Together they are named in 80 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2024 and Jun 3, 2026 — classified as 80 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (66 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 problems
Device problems
- Failure to Osseointegrate66
- Use of Device Problem15
Patient problems
- Insufficient Information80
CAMLOG SCREW-LINE Implant, Promote models
30 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CAMLOG® SCREW-LINE Implant, Promote® K1045.3809Implant, Endosseous, Root-Form8 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1045.4309Implant, Endosseous, Root-Form7 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.3813Implant, Endosseous, Root-Form6 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1045.5009Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.6009Implant, Endosseous, Root-Form5 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.3809Implant, Endosseous, Root-Form4 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.5009Implant, Endosseous, Root-Form4 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1045.3811Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1045.3813Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.3311Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.3313Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.4309Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1046.5011Implant, Endosseous, Root-Form3 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1042.5009Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1044.3311Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1044.3809Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1044.4311Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1045.3311Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1045.5013Implant, Endosseous, Root-Form2 reports
- CAMLOG® SCREW-LINE Implant, Promote® K1042.3311Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1042.4309Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1042.4313Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1042.4316Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1044.4309Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1044.5009Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1044.6009Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1045.4311Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1045.4313Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1046.4313Implant, Endosseous, Root-Form1 report
- CAMLOG® SCREW-LINE Implant, Promote® K1046.6011Implant, Endosseous, Root-Form1 report
Recent CAMLOG SCREW-LINE Implant, Promote adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 3, 2026Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25375286 ↗InjuryMay 20, 2026Failure to Osseointegrate
InjuryMay 20, 2026Failure to Osseointegrate
InjuryMay 13, 2026Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25160330 ↗InjuryMay 12, 2026Failure to Osseointegrate
InjuryApr 24, 2026Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 24984642 ↗InjuryApr 24, 2026Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 24979910 ↗InjuryApr 15, 2026Failure to Osseointegrate
InjuryDec 30, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 28, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 23, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 19, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryDec 19, 2025Use of Device Problem; Use of Device Problem
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 23848283 ↗InjuryNov 24, 2025Failure to Osseointegrate; Failure to Osseointegrate
InjuryOct 16, 2025Failure to Osseointegrate; Failure to Osseointegrate
Other ALTATEC GmbH products
- CONELOG PROGRESSIVE-LINE Implant, Promote plus36 models · 977 reports
- CAMLOG SCREW-LINE Implant, Promote plus60 models · 628 reports
- CAMLOG PROGRESSIVE-LINE Implant, Promote plus24 models · 219 reports
- CONELOG SCREW-LINE Implant, Promote plus44 models · 194 reports
- iSy Implants-Set17 models · 139 reports
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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