Touareg™-S Dental Implant 6.0D 10L ISPS1060Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 9
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 07290105151841), received between Jan 7, 2025 and Jul 10, 2026 — classified as 9 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (7 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 Problem7
- Fracture1
- Patient Device Interaction Problem1
Patient problems
- Inadequate Osseointegration5
- Pain4
- Failure of Implant2
- Bacterial Infection1
- Implant Pain1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjuryJul 10, 2026Osseointegration Problem
PAIN AND INFECTION 1 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25786736 ↗InjuryMay 26, 2026Osseointegration Problem
MOBILITY 9 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25279910 ↗InjuryFeb 4, 2026Osseointegration Problem
MOBILITY ONE MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24260615 ↗InjuryDec 8, 2025Fracture; Fracture
InjuryNov 21, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND MOBILITY 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 23623929 ↗InjuryJul 23, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY AND PAIN 6 MONTHS AFTER IMPLANTATION, DIABETIC PATIENT.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 22576991 ↗InjuryMay 25, 2025Osseointegration Problem; Osseointegration Problem
InjuryApr 25, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJan 7, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY LESS THAN A MONTH AFTER IMPLANTED, IMPLANT REMOVED AND GRAFTED, WILL RE IMPLANT IN 4 MONTHS.
Patient problems: Inadequate Osseointegration
MAUDE report 21094042 ↗
Other Implant, Endosseous, Root-Form devices
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- 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 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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