MIS Multi Unit MA-N1480Recalls & reported problems
MIS Implants Technologies Ltd. · Multi unit abutment 1mm, int. hex., NP · Class 2 · Implant
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07290108998801), received between May 6, 2026 and Jul 29, 2026 — classified as 4 injuries.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJul 29, 2026Fracture
It was reported that two straight multi-unit abutments fractured during function.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50068572 ↗InjuryJul 29, 2026Fracture
It was reported that two straight multi-unit abutments fractured during function.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50068494 ↗InjuryMay 6, 2026Fracture
A FRACTURE OF A NARROW MULTI-UNIT ABUTMENT WAS REPORTED, WITH AN APPLIED TORQUE OF 30 NCM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25104471 ↗InjuryMay 6, 2026Fracture
A FRACTURE OF A NARROW MULTI-UNIT ABUTMENT WAS REPORTED, WITH AN APPLIED TORQUE OF 30 NCM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25104461 ↗
Other Abutment, Implant, Dental, Endosseous devices
- CERTAIN® GOLD-TITE® IUNIHGZimVie US Corp LLC · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS151 reports
- Nobel Biocare® 36662Nobel Biocare AB · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS2 recalls5 reports
- 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.