Touareg™-X Dental Implant 5.0D 8L ISPX0850Recalls & reported problems
Adin Dental Implant Systems Ltd · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Adin Touareg-X dental implant is a root-form implant placed in the jawbone. Reports mostly describe implants that did not bond with bone or became loose months or years later, with mentions of infection, pain and bone loss. There are 25 reports that mention injury and no deaths. 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
- 24
- Deaths reported
- 0
- Injuries reported
- 24
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 24 adverse event reports that list this exact device (DI 07290105152176), received between Mar 18, 2025 and Jul 2, 2026 — classified as 24 injuries.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (11 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 Problem11
- Osseointegration Problem10
- Loss of Osseointegration3
Patient problems
- Inadequate Osseointegration15
- Bacterial Infection8
- Pain8
- Granuloma1
Recent adverse event reports
The 24 most recent of 24 reports, in the reporter's own words as published by the FDA.
InjuryJul 2, 2026Osseointegration Problem
MOBILITY ONE AND HALF YEAR AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25693498 ↗InjuryJun 12, 2026Loss of Osseointegration
INFECTION, PAIN AND BONE LOSS 8 YEARS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration; Pain
MAUDE report 25487044 ↗InjuryJun 5, 2026Patient Device Interaction Problem
InjuryMay 28, 2026Osseointegration Problem
InjuryMay 22, 2026Patient Device Interaction Problem
INFECTION 4 YEARS AND 7 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection
MAUDE report 25256977 ↗InjuryMay 19, 2026Osseointegration Problem
BONE LOSS A YEAR AND 8 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 25221643 ↗InjuryMay 12, 2026Loss of Osseointegration
INFECTION 4 YEARS AND 3 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection
MAUDE report 25149250 ↗InjuryApr 16, 2026Patient Device Interaction Problem
InjuryMar 23, 2026Patient Device Interaction Problem
PAIN AND INFECTION 2 WEEKS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 24664732 ↗InjuryMar 23, 2026Osseointegration Problem
MOBILITY I MONTH AND HALF AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24664727 ↗InjuryFeb 16, 2026Patient Device Interaction Problem
MOBILITY 2 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24345344 ↗InjuryFeb 16, 2026Osseointegration Problem
MOBILITY 4 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 24345318 ↗InjuryNov 25, 2025Osseointegration Problem; Osseointegration Problem
INFECTIONS AND MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Inadequate Osseointegration
MAUDE report 23650065 ↗InjuryNov 12, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 1 WEEK AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23534153 ↗InjuryNov 6, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 1 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 23487387 ↗InjuryAug 26, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY AND BONE LOSS 4 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22895427 ↗InjuryAug 20, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
INFECTION AND PAIN 1 MONTH AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 22854353 ↗InjuryAug 4, 2025Osseointegration Problem; Osseointegration Problem
PAIN AND BONE LOSS A YEAT AND 1 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 22705796 ↗InjuryJul 28, 2025Loss of Osseointegration; Loss of Osseointegration
MOBILITY 3 YEARS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22634270 ↗InjuryJul 28, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
InjuryJul 14, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
PAIN AND INFECTION 2 WEEKS AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Pain
MAUDE report 22495459 ↗InjuryJun 13, 2025Osseointegration Problem; Osseointegration Problem
INFECTION AND GRANULOMA A MONTH AFTER IMPLANTATION.
Patient problems: Bacterial Infection; Granuloma
MAUDE report 22202435 ↗InjuryJun 12, 2025Osseointegration Problem; Osseointegration Problem
MOBILITY 5 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 22195441 ↗InjuryMar 18, 2025Patient Device Interaction Problem; Patient Device Interaction Problem
MOBILITY 3 MONTHS AFTER IMPLANTATION.
Patient problems: Inadequate Osseointegration
MAUDE report 21631890 ↗
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
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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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