MIS C1Recalls & reported problems across all models
MIS Implants Technologies Ltd. · 22 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 18,138
- Deaths reported
- 0
- Injuries reported
- 18,136
- Recalls
- 0
We found 22 models of MIS C1 by MIS Implants Technologies Ltd. in the FDA's device registry (GUDID). Together they are named in 18,138 adverse event reports in the FDA's MAUDE database, received between Jul 16, 2024 and Sep 30, 2026 — classified as 18,136 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (11,094 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 C1 problems
Device problems
- Failure to Osseointegrate11,094
- Osseointegration Problem6,884
- Loss of Osseointegration152
- Fracture2
- Patient-Device Incompatibility2
- Adverse Event Without Identified Device or Use Problem1
- Fitting Problem1
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- Failure of Implant17,907
- No Clinical Signs, Symptoms or Conditions162
- Inadequate Osseointegration51
- Insufficient Information15
- Unspecified Infection10
- Osteolysis8
- Inflammation5
- Implant Pain2
MIS C1 models
22 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MIS C1 C1-10375Implant, Endosseous, Root-Form2,892 reports
- MIS C1 C1-10420Implant, Endosseous, Root-Form2,251 reports
- MIS C1 C1-11375Implant, Endosseous, Root-Form2,067 reports
- MIS C1 C1-08420Implant, Endosseous, Root-Form1,983 reports
- MIS C1 C1-08375Implant, Endosseous, Root-Form1,604 reports
- MIS C1 C1-13375Implant, Endosseous, Root-Form1,434 reports
- MIS C1 C1-11420Implant, Endosseous, Root-Form1,338 reports
- MIS C1 C1-10330Implant, Endosseous, Root-Form784 reports
- MIS C1 C1-13420Implant, Endosseous, Root-Form686 reports
- MIS C1 C1-08500Implant, Endosseous, Root-Form656 reports
- MIS C1 C1-10500Implant, Endosseous, Root-Form621 reports
- MIS C1 C1-11330Implant, Endosseous, Root-Form613 reports
- MIS C1 C1-13330Implant, Endosseous, Root-Form378 reports
- MIS C1 C1-16375Implant, Endosseous, Root-Form230 reports
- MIS C1 C1-11500Implant, Endosseous, Root-Form228 reports
- MIS C1 C1-16420Implant, Endosseous, Root-Form153 reports
- MIS C1 C1-13500Implant, Endosseous, Root-Form137 reports
- MIS C1 C1-16330Implant, Endosseous, Root-Form70 reports
- MIS C1 C1-16500Implant, Endosseous, Root-Form6 reports
- MIS C1 C1-X08420Implant, endosseous, root-form5 reports
- MIS C1 C1-X11375Implant, endosseous, root-form1 report
- MIS C1 C1-X13420Implant, endosseous, root-form1 report
Recent MIS C1 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
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 50944466 ↗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 50944172 ↗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 50944104 ↗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 50944012 ↗InjurySep 30, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss. No patient injury was reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50941583 ↗InjurySep 29, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937679 ↗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 50937314 ↗InjurySep 28, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration
MAUDE report 50921076 ↗InjurySep 28, 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 50915120 ↗InjurySep 28, 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 50913065 ↗InjurySep 28, 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 50912973 ↗InjurySep 28, 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 50912923 ↗InjurySep 28, 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 50912181 ↗InjurySep 27, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50909716 ↗InjurySep 27, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50909690 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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