ANKYLOS® 31024171Recalls & reported problems
Dentsply Implants Manufacturing GmbH · Regular C/ Abutment GH3.0/A7.5 · Class 2 · Implant
All models of ANKYLOS (112)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07392532217654), received between Jun 10, 2024 and Sep 10, 2026 — classified as 4 injuries, 1 malfunction.
The most frequently reported specific device problem is “Fracture” (4 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture4
- Loss of Osseointegration1
Patient problems
- Failure of Implant3
- Inadequate Osseointegration1
- No Clinical Signs, Symptoms or Conditions1
- Unspecified Infection1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjurySep 10, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss due to infection.
Patient problems: Inadequate Osseointegration; Unspecified Infection
MAUDE report 50714911 ↗InjuryJun 10, 2026Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FRACTURE.
Patient problems: Failure of Implant
MAUDE report 25453973 ↗InjuryJun 10, 2026Fracture
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FRACTURE.
Patient problems: Failure of Implant
MAUDE report 25453932 ↗MalfunctionJun 9, 2026Fracture
IT WAS REPORTED THAT THERE WAS A SCREW FRACTURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25446765 ↗InjuryJun 10, 2024Fracture; Fracture
IN THIS EVENT IT IS REPORTED THAT AN ANK REG C/ABUT GH 3,0 A 7,5 ABUTMENT FRACTURED. CASE DESCRIPTION IS SOMEWHAT UNCLEAR, BUT INDICATES, THAT THE IMPLANT REMAINS AS SLEEPER AFTER SEVERAL FAILED REPAIR ATTEMPTS.
Patient problems: Failure of Implant
MAUDE report 19498352 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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