MIS MA-SC248Recalls & reported problems
MIS Implants Technologies Ltd. · Straight Multi unit abutment, H2mm, concave, int. hex., SP · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07290109005607), received between Mar 26, 2026 and Mar 26, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Mechanical Problem” (1 report).
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
- Mechanical Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 26, 2026Mechanical Problem
IT WAS REPORTED THAT IN ORDER TO PLACE THE SCAN POST INTO THE MULTI-UNIT ABUTMENT (MA-SC248), REMOVAL OF THE HEALING CAP (MU-H4480) WAS ATTEMPTED. DURING THIS ATTEMPT, THE MULTI-UNIT ABUTMENT CAME OFF THE IMPLANT TOGETHER WITH THE HEALING CAP, AND THE COMPONENTS COULD NOT BE SEPARATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24703016 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.