ANKYLOSRecalls & reported problems across all models
Dentsply Implants Manufacturing GmbH · 112 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
ANKYLOS models — page 2
112 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ANKYLOS® 31037500Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31037543Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31047046Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31056200IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31056301IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31010420IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31010422IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31010423IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31010428IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021670IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021680IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31056021IMPLANT, 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.
How reports and recalls are matched · Editorial policy · Report an error on this page