MIS CK-SLC4Recalls & reported problems
MIS Implants Technologies Ltd. · LOCKiT abutment kit, H4mm, coni. con., SP · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07290109009940), received between Apr 30, 2026 and Apr 30, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (2 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- Failure of Implant2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 30, 2026Fracture
IT WAS REPORTED THAT WEAR WAS OBSERVED IN TWO LOCKIT ABUTMENTS, WHICH HAVE BEEN IN USE SINCE 2023.
Patient problems: Failure of Implant
MAUDE report 25042388 ↗InjuryApr 30, 2026Fracture
IT WAS REPORTED THAT WEAR WAS OBSERVED IN TWO LOCKIT ABUTMENTS, WHICH HAVE BEEN IN USE SINCE 2023.
Patient problems: Failure of Implant
MAUDE report 25042341 ↗
Other Abutment, implant, dental, endosseous devices
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- CERTAIN® IUNIHTZimVie US Corp LLC · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS67 reports
- ATLANTIS® 35502Dentsply Ih, Inc. · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS66 reports
- ATLANTIS® 35502Dentsply Ih, Inc. · Abutment, implant, dental, endosseous54 reports
- Esthetic Abutment 36669Nobel Biocare AB · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall2 reports
- CERTAIN® BELLATEK® IEDAT5ZimVie US Corp LLC · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall1 report
- Custom Abutments Final AbutmentsInstitut Straumann AG · Abutment, implant, dental, endosseous1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.