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
- Adverse event reports
- 20,917
- Deaths reported
- 0
- Injuries reported
- 20,843
- Recalls
- 0
We found 112 models of ANKYLOS by Dentsply Implants Manufacturing GmbH in the FDA's device registry (GUDID). Together they are named in 20,917 adverse event reports in the FDA's MAUDE database, received between Dec 7, 2022 and Sep 30, 2026 — classified as 20,843 injuries, 74 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (12,096 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 ANKYLOS problems
Device problems
- Failure to Osseointegrate12,096
- Loss of Osseointegration7,225
- Fracture1,513
- Damaged Thread50
- Separation Failure31
- Malposition of Device25
- Off-Label Use16
- Insufficient Device Problem Information15
Patient problems
- Failure of Implant20,289
- Unspecified Infection3,765
- Inflammation2,970
- Osteolysis1,910
- Pocket Erosion1,332
- No Clinical Signs, Symptoms or Conditions395
- Inadequate Osseointegration217
- Implant Pain122
ANKYLOS models
112 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ANKYLOS® 31010408IMPLANT, ENDOSSEOUS, ROOT-FORM4,846 reports
- ANKYLOS® 31010410IMPLANT, ENDOSSEOUS, ROOT-FORM4,666 reports
- ANKYLOS® 31010405IMPLANT, ENDOSSEOUS, ROOT-FORM2,916 reports
- ANKYLOS® 31010428IMPLANT, ENDOSSEOUS, ROOT-FORM2,058 reports
- ANKYLOS® 31010425IMPLANT, ENDOSSEOUS, ROOT-FORM1,747 reports
- ANKYLOS® 31010430IMPLANT, ENDOSSEOUS, ROOT-FORM1,275 reports
- ANKYLOS® 31010420IMPLANT, ENDOSSEOUS, ROOT-FORM1,065 reports
- ANKYLOS® 31010403IMPLANT, ENDOSSEOUS, ROOT-FORM652 reports
- ANKYLOS® 31010423IMPLANT, ENDOSSEOUS, ROOT-FORM520 reports
- ANKYLOS® 31010440IMPLANT, ENDOSSEOUS, ROOT-FORM249 reports
- ANKYLOS® 31010453IMPLANT, ENDOSSEOUS, ROOT-FORM148 reports
- ANKYLOS® 31010455IMPLANT, ENDOSSEOUS, ROOT-FORM124 reports
- ANKYLOS® 31010458IMPLANT, ENDOSSEOUS, ROOT-FORM99 reports
- ANKYLOS® 31010422IMPLANT, ENDOSSEOUS, ROOT-FORM51 reports
- ANKYLOS® 31010452IMPLANT, ENDOSSEOUS, ROOT-FORM42 reports
- ANKYLOS® 31021640IMPLANT, ENDOSSEOUS, ROOT-FORM28 reports
- ANKYLOS® 31024170IMPLANT, ENDOSSEOUS, ROOT-FORM28 reports
- ANKYLOS® 31024160IMPLANT, ENDOSSEOUS, ROOT-FORM22 reports
- ANKYLOS® 31010472IMPLANT, ENDOSSEOUS, ROOT-FORM21 reports
- ANKYLOS® 31024180IMPLANT, ENDOSSEOUS, ROOT-FORM17 reports
- ANKYLOS® 31056021IMPLANT, ENDOSSEOUS, ROOT-FORM17 reports
- ANKYLOS® 31024130IMPLANT, ENDOSSEOUS, ROOT-FORM16 reports
- ANKYLOS® 31024120IMPLANT, ENDOSSEOUS, ROOT-FORM15 reports
- ANKYLOS® 31056022IMPLANT, ENDOSSEOUS, ROOT-FORM15 reports
- ANKYLOS® 31010460IMPLANT, ENDOSSEOUS, ROOT-FORM13 reports
- ANKYLOS® 31010410IMPLANT, ENDOSSEOUS, ROOT-FORM13 reports
- ANKYLOS® 31010474IMPLANT, ENDOSSEOUS, ROOT-FORM12 reports
- ANKYLOS® 31021630IMPLANT, ENDOSSEOUS, ROOT-FORM11 reports
- ANKYLOS® 31022530IMPLANT, ENDOSSEOUS, ROOT-FORM11 reports
- ANKYLOS® 31021100IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- ANKYLOS® 31024172IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- ANKYLOS® 31010408IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- ANKYLOS® 31010450IMPLANT, ENDOSSEOUS, ROOT-FORM9 reports
- ANKYLOS® 31010425IMPLANT, ENDOSSEOUS, ROOT-FORM8 reports
- ANKYLOS® 31021076IMPLANT, ENDOSSEOUS, ROOT-FORM7 reports
- ANKYLOS® 31024161IMPLANT, ENDOSSEOUS, ROOT-FORM6 reports
- ANKYLOS® 31010470IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31021120IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31021625IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31021645IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31021660IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31022540IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31024122IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31024132IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31024171IMPLANT, ENDOSSEOUS, ROOT-FORM5 reports
- ANKYLOS® 31021110IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- ANKYLOS® 31021649IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- ANKYLOS® 31024016IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- ANKYLOS® 31024150IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- ANKYLOS® 31010430IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- ANKYLOS® 31010130IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31021060IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31021200IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31022520IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31022542ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS3 reports
- ANKYLOS® 31022550IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31022556ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS3 reports
- ANKYLOS® 31024112IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31024121IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31024131IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31024182IMPLANT, ENDOSSEOUS, ROOT-FORM3 reports
- ANKYLOS® 31021050IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31021070IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31021190IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31021300IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31021550IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31021647IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31021650IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31024014IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31024110IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31024152IMPLANT, ENDOSSEOUS, ROOT-FORM2 reports
- ANKYLOS® 31033623Accessories, implant, dental, endosseous2 reports
- ANKYLOS® 31010481IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31010476IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021080IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021090IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021140IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021310IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021312IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021320IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021321IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021515IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021535IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31021665IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31022120ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 report
- ANKYLOS® 31022134ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 report
- ANKYLOS® 31022512IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31023030ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 report
- ANKYLOS® 31023310ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 report
- ANKYLOS® 31024140IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31024141IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31024153IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31024162IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31024181IMPLANT, ENDOSSEOUS, ROOT-FORM1 report
- ANKYLOS® 31033456Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31034660Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31037043Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31037044Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31037053Accessories, implant, dental, endosseous1 report
- ANKYLOS® 31037209Accessories, implant, dental, endosseous1 report
Recent ANKYLOS adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50955148 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration; Inflammation
MAUDE report 50954458 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954280 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: Inadequate Osseointegration
MAUDE report 50953995 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953733 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953601 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953409 ↗InjurySep 30, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952640 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration; Osteolysis
MAUDE report 50952466 ↗InjurySep 30, 2026Fracture
It was reported that a patient experienced a dental implant fracture and the implant was removed.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951731 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950860 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration
MAUDE report 50950836 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration
MAUDE report 50950730 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration; Unspecified Infection
MAUDE report 50950155 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration
MAUDE report 50949132 ↗
Other Dentsply Implants Manufacturing GmbH products
- ASTRA TECH Implant System EV177 models · 37,200 reports
- ASTRA TECH Implant System166 models · 27,749 reports
- XiVE62 models · 12,456 reports
- DS PrimeTaper61 models · 6,897 reports
- DS OmniTaper32 models · 2,128 reports
- DS Implants44 models · 145 reports
- FRIADENT23 models · 55 reports
- FRIALIT12 models · 35 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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