MIS LANCERecalls & reported problems across all models
MIS Implants Technologies Ltd. · 14 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 210
- Deaths reported
- 0
- Injuries reported
- 210
- Recalls
- 0
We found 14 models of MIS LANCE by MIS Implants Technologies Ltd. in the FDA's device registry (GUDID). Together they are named in 210 adverse event reports in the FDA's MAUDE database, received between Aug 8, 2024 and Aug 4, 2026 — classified as 210 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (153 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 LANCE problems
Device problems
- Osseointegration Problem153
- Failure to Osseointegrate57
Patient problems
- Failure of Implant210
MIS LANCE models
14 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MIS LANCE EF5-11420Implant, Endosseous, Root-Form39 reports
- MIS LANCE EF5-10375Implant, Endosseous, Root-Form32 reports
- MIS LANCE EF5-10420Implant, Endosseous, Root-Form30 reports
- MIS LANCE EF5-11375Implant, Endosseous, Root-Form26 reports
- MIS LANCE EF5-13420Implant, Endosseous, Root-Form19 reports
- MIS LANCE EF5-13375Implant, Endosseous, Root-Form16 reports
- MIS LANCE EF5-08375Implant, Endosseous, Root-Form13 reports
- MIS LANCE EF5-08420Implant, Endosseous, Root-Form12 reports
- MIS LANCE EF5-10500Implant, Endosseous, Root-Form8 reports
- MIS LANCE EF5-16375Implant, Endosseous, Root-Form6 reports
- MIS LANCE EF5-08500Implant, Endosseous, Root-Form5 reports
- MIS LANCE EF5-13500Implant, Endosseous, Root-Form2 reports
- MIS LANCE EF5-16500Implant, Endosseous, Root-Form1 report
- MIS LANCE EF5-16420Implant, Endosseous, Root-Form1 report
Recent MIS LANCE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 4, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50132418 ↗InjuryAug 4, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50132337 ↗InjuryAug 4, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50132209 ↗InjuryAug 4, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50132125 ↗InjuryAug 4, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50131950 ↗InjuryAug 4, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50131909 ↗InjuryJun 29, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25652220 ↗InjuryJun 9, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25445529 ↗InjuryJun 9, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25444989 ↗InjuryMay 5, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25082963 ↗InjuryMay 5, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25082962 ↗InjuryMay 5, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25082938 ↗InjuryMay 4, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25068104 ↗InjuryApr 30, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25039376 ↗InjuryApr 20, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 24928388 ↗
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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