CAMLOG PROGRESSIVE-LINE Implant, Promote plusRecalls & reported problems across all models
ALTATEC GmbH · 24 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 219
- Deaths reported
- 0
- Injuries reported
- 219
- Recalls
- 0
We found 24 models of CAMLOG PROGRESSIVE-LINE Implant, Promote plus by ALTATEC GmbH in the FDA's device registry (GUDID). Together they are named in 219 adverse event reports in the FDA's MAUDE database, received between Mar 22, 2024 and Jul 9, 2026 — classified as 219 injuries.
The most frequently reported specific device problem is “Use of Device Problem” (125 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 PROGRESSIVE-LINE Implant, Promote plus problems
Device problems
- Use of Device Problem125
- Failure to Osseointegrate115
- Device Handling Problem4
- Use of Incorrect Control/Treatment Settings2
- Fracture1
- Loss of Osseointegration1
Patient problems
- Insufficient Information219
CAMLOG PROGRESSIVE-LINE Implant, Promote plus models
24 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.4309Implant, Endosseous, Root-Form43 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.3809Implant, Endosseous, Root-Form39 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.4311Implant, Endosseous, Root-Form30 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.3811Implant, Endosseous, Root-Form19 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.3813Implant, Endosseous, Root-Form11 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.4309Implant, Endosseous, Root-Form9 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.4311Implant, Endosseous, Root-Form7 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.3311Implant, Endosseous, Root-Form6 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.3811Implant, Endosseous, Root-Form6 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.3313Implant, Endosseous, Root-Form5 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.5009Implant, Endosseous, Root-Form5 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.4313Implant, Endosseous, Root-Form5 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.5011Implant, Endosseous, Root-Form4 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.5013Implant, Endosseous, Root-Form4 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.3311Implant, Endosseous, Root-Form4 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.4313Implant, Endosseous, Root-Form3 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.3313Implant, Endosseous, Root-Form3 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.3809Implant, Endosseous, Root-Form3 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.3813Implant, Endosseous, Root-Form3 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.5009Implant, Endosseous, Root-Form3 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.5011Implant, Endosseous, Root-Form3 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.3816Implant, Endosseous, Root-Form2 reports
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1075.4316Implant, Endosseous, Root-Form1 report
- CAMLOG® PROGRESSIVE-LINE Implant, Promote® plus K1076.5013Implant, Endosseous, Root-Form1 report
Recent CAMLOG 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 9, 2026Failure to Osseointegrate
InjuryJul 8, 2026Failure to Osseointegrate
InjuryJun 16, 2026Failure to Osseointegrate
InjuryJun 16, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25381858 ↗InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25377054 ↗InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 3, 2026Use of Device Problem; Failure to Osseointegrate
IMPLANT REMOVED DUE TO SURGICAL CONSIDERATION WITHIN 36 HOURS.
Patient problems: Insufficient Information
MAUDE report 25375402 ↗InjuryJun 3, 2026Failure to Osseointegrate
InjuryJun 2, 2026Failure to Osseointegrate
InjuryMay 29, 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.
How reports and recalls are matched · Editorial policy · Report an error on this page