MIS CN-HS640Recalls & reported problems
MIS Implants Technologies Ltd. · Healing cap Ø4x6mm coni. con., NP · 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 07290108995978), received between Apr 7, 2026 and Apr 17, 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
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 17, 2026Fracture
CUSTOMER REPORTED THAT THE HEALING CAP BROKE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24913172 ↗InjuryApr 7, 2026Fracture
THE CUSTOMER REPORTED THAT THE ABUTMENT SCREW FRACTURED INSIDE A C1 IMPLANT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24796507 ↗
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- Esthetic Abutment 36669Nobel Biocare AB · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall2 reports
- CERTAIN® BELLATEK® IEDAT5ZimVie US Corp LLC · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall1 report
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.