MIS SEVEN MF7-08600Recalls & reported problems
MIS Implants Technologies Ltd. · Seven internal hex. implant dia.6 L 8mm · Class 2 · Implant
Quick summary
This MIS Seven dental implant is a screw-shaped implant placed in the jawbone to support a replacement tooth. Of the 162 reports, most describe implants that did not fuse with the jawbone or were lost after placement. The reports include no deaths and 162 injuries, and reports fell to 35 in the last 12 months from 73 before. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 167
- Deaths reported
- 0
- Injuries reported
- 167
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 167 adverse event reports that list this exact device (DI 07290108996432), received between Aug 8, 2024 and Sep 17, 2026 — classified as 167 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (91 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
- Failure to Osseointegrate91
- Osseointegration Problem70
- Loss of Osseointegration6
Patient problems
- Failure of Implant161
- Inadequate Osseointegration6
- Osteolysis3
- Deformity/ Disfigurement1
Recent adverse event reports
The 25 most recent of 167 reports, in the reporter's own words as published by the FDA.
InjurySep 17, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration; Osteolysis
MAUDE report 50812424 ↗InjurySep 17, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration
MAUDE report 50812001 ↗InjurySep 17, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration; Osteolysis
MAUDE report 50811710 ↗InjurySep 17, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration; Osteolysis
MAUDE report 50811375 ↗InjurySep 17, 2026Loss of Osseointegration
Patient problems: Inadequate Osseointegration
MAUDE report 50811233 ↗InjurySep 10, 2026Loss of Osseointegration
It was reported that a patient experienced a dental implant loss.
Patient problems: Inadequate Osseointegration
MAUDE report 50718016 ↗InjuryAug 3, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50116380 ↗InjuryJul 28, 2026Failure to Osseointegrate
It was reported that a patient experienced a dental implant loss.
Patient problems: Failure of Implant
MAUDE report 50058821 ↗InjuryJul 10, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25777934 ↗InjuryJun 8, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25433539 ↗InjuryJun 8, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25428860 ↗InjuryApr 27, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 25008032 ↗InjuryApr 27, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant
MAUDE report 25007251 ↗InjuryApr 6, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 24795907 ↗InjuryMar 7, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant
MAUDE report 24541146 ↗InjuryFeb 16, 2026Failure to Osseointegrate
MIS WARRANTY. COSTUMER REPORTED IMPLANT FAILURE. (B)(6). OVER 30 DAY POLICY - UNABLE TO SEND REPLACEMENT.
Patient problems: Failure of Implant
MAUDE report 24357520 ↗InjuryFeb 16, 2026Failure to Osseointegrate
MIS WARRANTY COSTUMER REPORTED IMPLANT FAILURE SF 04778756 OVER 30 DAY POLICY - UNABLE TO SEND REPLACEMENT.
Patient problems: Failure of Implant
MAUDE report 24356228 ↗InjuryFeb 16, 2026Failure to Osseointegrate
MIS WARRANTY IMPLANT FAILURE SF 04778756 OVER 30 DAY POLICY - UNABLE TO SEND REPLACEMENT.
Patient problems: Failure of Implant
MAUDE report 24355517 ↗InjuryFeb 10, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant
MAUDE report 24309767 ↗InjuryFeb 9, 2026Failure to Osseointegrate
MIS WARRANTY: COSTUMER REPORTED IMPLANT FAILURE: SF (B)(4). OVER 30 DAY POLICY - UNABLE TO SEND REPLACEMENT.
Patient problems: Failure of Implant
MAUDE report 24292388 ↗InjuryFeb 9, 2026Failure to Osseointegrate
MIS WARRANTY. COSTUMER REPORTED IMPLANT FAILURE. (B)(6). OVER 30 DAY POLICY - UNABLE TO SEND REPLACEMENT.
Patient problems: Failure of Implant
MAUDE report 24292286 ↗InjuryFeb 6, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 24278029 ↗InjuryFeb 6, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 24275334 ↗InjuryFeb 3, 2026Failure to Osseointegrate
Patient problems: Failure of Implant
MAUDE report 24250267 ↗InjuryFeb 2, 2026Failure to Osseointegrate
IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.
Patient problems: Failure of Implant
MAUDE report 24233186 ↗
Other Implant, Endosseous, Root-Form devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.