Replace SelectRecalls & reported problems across all models
Nobel Biocare AB · 107 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Replace Select models — page 2
107 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Replace Select™ 36289IMPLANT, ENDOSSEOUS, ROOT-FORM22 reports
- Replace Select™ 36110IMPLANT, ENDOSSEOUS, ROOT-FORM17 reports
- Replace Select™ 37314IMPLANT, ENDOSSEOUS, ROOT-FORM16 reports
- Replace® Select 28955IMPLANT, ENDOSSEOUS, ROOT-FORM12 reports
- Replace Select™ 37319IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- Replace Select™ 37319IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- Replace Select™ 37318IMPLANT, ENDOSSEOUS, ROOT-FORM8 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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