Touareg CloseFit™ RP Dental Implant 3.5D 10L ISPX1035Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 14
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 07290105152190), received between Jan 29, 2025 and Jun 15, 2026 — classified as 14 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
- Patient Device Interaction Problem4
- Loss of Osseointegration2
- Fracture1
Patient problems
- Inadequate Osseointegration9
- Pain5
- Bacterial Infection4
- Failure of Implant2
- Unspecified Infection1
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
InjuryJun 15, 2026Osseointegration Problem
PAIN AND INFECTION 3 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 25503020 ↗InjuryMay 1, 2026Patient Device Interaction Problem
PAIN AND MOBILITY 2 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 25058014 ↗InjuryJan 20, 2026Patient Device Interaction Problem
InjuryAug 26, 2025Loss of Osseointegration; Loss of Osseointegration
PAIN AND MOBILITY 2 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 22895697 ↗InjuryJul 31, 2025Fracture; Fracture
InjuryJul 11, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22485167 ↗InjuryJul 11, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 3 WEEKS AFTER IMPLANTATION. PATIENT WITH HYPERTENSION.
Patient problems: Inadequate Osseointegration
MAUDE report 22485159 ↗InjuryJul 11, 2025Osseointegration Problem; Osseointegration Problem
INFECTION A MONTH AFTER IMPLANTATION. DIABETIC PATIENT.
Patient problems: Bacterial Infection
MAUDE report 22485155 ↗InjuryJun 18, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
DENTAL IMPLANT FAILURE.
Patient problems: Failure of Implant; Unspecified Infection
MAUDE report 22283106 ↗InjuryFeb 7, 2025Loss of Osseointegration; Loss of Osseointegration
BONE LOSS ONE YEAR AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21337304 ↗InjuryFeb 6, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 4 MOTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21326973 ↗InjuryFeb 6, 2025Osseointegration Problem; Osseointegration Problem
PAIN, MOBILITY AND INFECTION 4 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Pain
MAUDE report 21326951 ↗InjuryFeb 6, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY AND INFECTION A MONTH AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 21326948 ↗InjuryJan 29, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 5 MONTH AFTER IMPLANTANTION.
Patient problems: Inadequate Osseointegration
MAUDE report 21266692 ↗
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- 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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