Brånemark SystemRecalls & reported problems across all models
Nobel Biocare AB · 141 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Brånemark System models — page 2
141 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Brånemark System® 34738IMPLANT, ENDOSSEOUS, ROOT-FORM18 reports
- Brånemark System® 28891IMPLANT, ENDOSSEOUS, ROOT-FORM16 reports
- Brånemark System® 28917IMPLANT, ENDOSSEOUS, ROOT-FORM16 reports
- Brånemark System® 28864IMPLANT, ENDOSSEOUS, ROOT-FORM15 reports
- Brånemark System® 28884IMPLANT, ENDOSSEOUS, ROOT-FORM14 reports
- Brånemark System® 34723IMPLANT, ENDOSSEOUS, ROOT-FORM14 reports
- Brånemark System® 28864IMPLANT, ENDOSSEOUS, ROOT-FORM12 reports
- Brånemark System® 32124IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- Brånemark System® 28896IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- Brånemark System® 28898IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- Brånemark System® 28867IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- Brånemark System® 28883IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28888IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28899IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28900IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28944IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28863IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28865IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28866IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 28888IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Brånemark System® 32131IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28930IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28893IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28894IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28897IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28901IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28867IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28924IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- Brånemark System® 28866IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- Brånemark System® 28924IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 28879IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 28890IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 28868IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 28868IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 28869IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 34740IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- Brånemark System® 28880IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- Brånemark System® 28889IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- Brånemark System® 28869IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- Brånemark System® 28863IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- Brånemark System® 28862IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
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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