Touareg CloseFit™ NP Dental Implant 3.0D 11.5L ISPNP1130Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07290105151681), received between Jan 5, 2026 and Sep 9, 2026 — classified as 7 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (3 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Osseointegration Problem3
- Patient Device Interaction Problem3
- Detachment of Device or Device Component1
- Difficult to Insert1
Patient problems
- Inadequate Osseointegration5
- Bacterial Infection2
- Failure of Implant1
- Pain1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
InjurySep 9, 2026Difficult to Insert; Detachment of Device or Device Component
InjuryMay 28, 2026Osseointegration Problem
MOBILITY 1 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25318406 ↗InjuryMay 19, 2026Osseointegration Problem
BONE LOSS AND INFECTION 5 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 25219667 ↗InjuryMay 13, 2026Osseointegration Problem
MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25162752 ↗InjuryApr 7, 2026Patient Device Interaction Problem
MOBILITY ONE MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24807792 ↗InjuryJan 5, 2026Patient Device Interaction Problem
PAIN AND INFECTION 2 WEEKS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 23957949 ↗InjuryJan 5, 2026Patient Device Interaction Problem
MOBILITY 2 WEEKS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23957884 ↗
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- 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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