MIS SEVENRecalls & reported problems across all models
MIS Implants Technologies Ltd. · 29 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 28,982
- Deaths reported
- 0
- Injuries reported
- 28,981
- Recalls
- 0
We found 29 models of MIS SEVEN by MIS Implants Technologies Ltd. in the FDA's device registry (GUDID). Together they are named in 28,982 adverse event reports in the FDA's MAUDE database, received between Aug 8, 2024 and Sep 30, 2026 — classified as 28,981 injuries, 1 malfunction.
The most frequently reported specific device problem is “Osseointegration Problem” (16,911 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported MIS SEVEN problems
Device problems
- Osseointegration Problem16,911
- Failure to Osseointegrate11,870
- Loss of Osseointegration185
- Fracture13
- Patient-Device Incompatibility2
- Difficult to Insert1
- Naturally Worn1
Patient problems
- Failure of Implant28,792
- No Clinical Signs, Symptoms or Conditions131
- Inadequate Osseointegration53
- Inflammation20
- Osteolysis20
- Unspecified Infection12
- Deformity/ Disfigurement10
- Insufficient Information7
MIS SEVEN models
29 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MIS SEVEN MF7-10375Implant, Endosseous, Root-Form4,560 reports
- MIS SEVEN MF7-11375Implant, Endosseous, Root-Form3,592 reports
- MIS SEVEN MF7-10420Implant, Endosseous, Root-Form3,427 reports
- MIS SEVEN MF7-08375Implant, Endosseous, Root-Form2,549 reports
- MIS SEVEN MF7-08420Implant, Endosseous, Root-Form2,030 reports
- MIS SEVEN MF7-11420Implant, Endosseous, Root-Form1,844 reports
- MIS SEVEN MF7-13375Implant, Endosseous, Root-Form1,677 reports
- MIS SEVEN MF7-10330Implant, Endosseous, Root-Form1,450 reports
- MIS SEVEN MF7-10500Implant, Endosseous, Root-Form1,174 reports
- MIS SEVEN MF7-11330Implant, Endosseous, Root-Form1,052 reports
- MIS SEVEN MF7-13420Implant, Endosseous, Root-Form977 reports
- MIS SEVEN MF7-08500Implant, Endosseous, Root-Form952 reports
- MIS SEVEN MF7-06420Implant, Endosseous, Root-Form854 reports
- MIS SEVEN MF7-13330Implant, Endosseous, Root-Form594 reports
- MIS SEVEN MF7-11500Implant, Endosseous, Root-Form539 reports
- MIS SEVEN MF7-06500Implant, Endosseous, Root-Form373 reports
- MIS SEVEN MF7-16375Implant, Endosseous, Root-Form313 reports
- MIS SEVEN MF7-13500Implant, Endosseous, Root-Form240 reports
- MIS SEVEN MF7-16420Implant, Endosseous, Root-Form204 reports
- MIS SEVEN MF7-08600Implant, Endosseous, Root-Form167 reports
- MIS SEVEN MF7-10600Implant, Endosseous, Root-Form110 reports
- MIS SEVEN MF7-06600Implant, Endosseous, Root-Form107 reports
- MIS SEVEN MF7-16330Implant, Endosseous, Root-Form60 reports
- MIS SEVEN MF7-11600Implant, Endosseous, Root-Form56 reports
- MIS SEVEN MF7-13600Implant, Endosseous, Root-Form44 reports
- MIS SEVEN MF7-16500Implant, Endosseous, Root-Form28 reports
- MIS SEVEN MG7-11330Implant, Endosseous, Root-Form6 reports
- MIS SEVEN MG7-10330Implant, Endosseous, Root-Form2 reports
- MIS SEVEN MG7-13330Implant, Endosseous, Root-Form1 report
Recent MIS SEVEN adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions; Osteolysis
MAUDE report 50954152 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration
MAUDE report 50951825 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50951813 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration
MAUDE report 50948154 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944491 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944434 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944365 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944352 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50943991 ↗InjurySep 30, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50943984 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50941779 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50941625 ↗MalfunctionSep 29, 2026Difficult to Insert
Patient problems: Insufficient Information
MAUDE report 50937411 ↗InjurySep 29, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933163 ↗InjurySep 29, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss. There was no reported injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931232 ↗
Other MIS Implants Technologies Ltd. products
All MIS Implants Technologies Ltd. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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