Touareg CloseFit™ WP Dental Implant 5D 8.0L ISPX0849Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 07290105152169), received between Jun 2, 2025 and May 13, 2026 — classified as 10 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (6 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
- Patient Device Interaction Problem6
- Osseointegration Problem4
Patient problems
- Inadequate Osseointegration7
- Bacterial Infection4
- Granuloma1
- Pain1
- Sinus Perforation1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
InjuryMay 13, 2026Patient Device Interaction Problem
InjuryMar 30, 2026Patient Device Interaction Problem
MOBILITY AND PAIN 20 DAYS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 24728911 ↗InjuryMar 23, 2026Osseointegration Problem
MOBILITY 6 MONTH AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664756 ↗InjuryMar 23, 2026Osseointegration Problem
MOBILITY 7 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664747 ↗InjuryDec 18, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
SINUS PENETRATION, INFECTION 28 DAYS AFTER IMPLANTATION
Patient problems: Bacterial Infection; Inadequate Osseointegration; Sinus Perforation
MAUDE report 23838563 ↗InjuryAug 26, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 1 DAY AFTER IMPLANTATION. PATIENT WITH CARDIAC DISEASE.
Patient problems: Inadequate Osseointegration
MAUDE report 22895678 ↗InjuryAug 20, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
SCAR TISSUE 2 DAYS AFTER IMPLANTATION, PATIENT WITH DIABETES AND CARDIAC PROBLEMS.
Patient problems: Granuloma
MAUDE report 22854339 ↗InjuryJul 11, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 5 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22485161 ↗InjuryJun 3, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
INFECTION 3 DAYS AFTER IMPLANTATION, PATIENT WITH HYPERTENSION.
Patient problems: Bacterial Infection
MAUDE report 22135806 ↗InjuryJun 2, 2025Osseointegration Problem; Osseointegration Problem
BONE LOSS AND INFECTION 6 MONTH AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 22124075 ↗
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- 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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