SPI CONTACT INICELLRecalls & reported problems across all models
Thommen Medical AG · 37 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1,771
- Deaths reported
- 0
- Injuries reported
- 1,771
- Recalls
- 0
We found 37 models of SPI CONTACT INICELL by Thommen Medical AG in the FDA's device registry (GUDID). Together they are named in 1,771 adverse event reports in the FDA's MAUDE database, received between Jan 7, 2018 and Aug 28, 2026 — classified as 1,771 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (1,419 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported SPI CONTACT INICELL problems
Device problems
- Failure to Osseointegrate1,419
- Loss of Osseointegration347
- Break3
- Adverse Event Without Identified Device or Use Problem2
- Unstable1
Patient problems
- Inadequate Osseointegration1,158
- No Code Available611
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
SPI CONTACT INICELL models
37 models, most reported first. Each model has its own page with its reports, recalls and device details.
- SPI CONTACT INICELL 4.23.624Implant, Endosseous, Root-Form289 reports
- SPI CONTACT INICELL 4.23.223Implant, Endosseous, Root-Form164 reports
- SPI CONTACT INICELL 4.23.233Implant, Endosseous, Root-Form131 reports
- SPI CONTACT INICELL 4.23.634Implant, Endosseous, Root-Form109 reports
- SPI CONTACT INICELL 4.23.224Implant, Endosseous, Root-Form106 reports
- SPI CONTACT INICELL 4.23.214Implant, Endosseous, Root-Form105 reports
- SPI CONTACT INICELL 4.23.615Implant, Endosseous, Root-Form91 reports
- SPI CONTACT INICELL 4.23.625Implant, Endosseous, Root-Form89 reports
- SPI CONTACT INICELL 4.23.243Implant, Endosseous, Root-Form77 reports
- SPI CONTACT INICELL 4.23.234Implant, Endosseous, Root-Form63 reports
- SPI CONTACT INICELL 4.23.644Implant, Endosseous, Root-Form59 reports
- SPI CONTACT INICELL 4.23.235Implant, Endosseous, Root-Form48 reports
- SPI CONTACT INICELL 4.23.225Implant, Endosseous, Root-Form46 reports
- SPI CONTACT INICELL 4.23.244Implant, Endosseous, Root-Form42 reports
- SPI CONTACT INICELL 4.23.253Implant, Endosseous, Root-Form41 reports
- SPI CONTACT INICELL 4.23.635Implant, Endosseous, Root-Form38 reports
- SPI CONTACT INICELL 4.23.616Implant, Endosseous, Root-Form36 reports
- SPI CONTACT INICELL 4.23.626Implant, Endosseous, Root-Form27 reports
- SPI CONTACT INICELL 4.23.215Implant, Endosseous, Root-Form26 reports
- SPI CONTACT INICELL 4.23.236Implant, Endosseous, Root-Form22 reports
- SPI CONTACT INICELL 4.23.254Implant, Endosseous, Root-Form20 reports
- SPI CONTACT INICELL 4.23.645Implant, Endosseous, Root-Form18 reports
- SPI CONTACT INICELL 4.23.636Implant, Endosseous, Root-Form18 reports
- SPI CONTACT INICELL 4.23.226Implant, Endosseous, Root-Form16 reports
- SPI CONTACT INICELL 4.23.216Implant, Endosseous, Root-Form14 reports
- SPI CONTACT INICELL 4.23.654Implant, Endosseous, Root-Form13 reports
- SPI CONTACT INICELL 4.23.255Implant, Endosseous, Root-Form12 reports
- SPI CONTACT INICELL 4.23.245Implant, Endosseous, Root-Form10 reports
- SPI CONTACT INICELL 4.23.646Implant, Endosseous, Root-Form9 reports
- SPI CONTACT INICELL 4.23.256Implant, Endosseous, Root-Form9 reports
- SPI CONTACT INICELL 4.23.617Implant, Endosseous, Root-Form6 reports
- SPI CONTACT INICELL 4.23.246Implant, Endosseous, Root-Form5 reports
- SPI CONTACT INICELL 4.23.627Implant, Endosseous, Root-Form4 reports
- SPI CONTACT INICELL 4.23.655Implant, Endosseous, Root-Form3 reports
- SPI CONTACT INICELL 4.23.637Implant, Endosseous, Root-Form2 reports
- SPI CONTACT INICELL 4.23.237Implant, Endosseous, Root-Form2 reports
- SPI CONTACT INICELL 4.23.656Implant, Endosseous, Root-Form1 report
Recent SPI CONTACT INICELL adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryAug 28, 2026Failure to Osseointegrate
Implant didn't achieve osseointegration.
Patient problems: Inadequate Osseointegration
MAUDE report 50492838 ↗InjuryAug 28, 2026Failure to Osseointegrate
Implant didn't achieve osseointegration, no thread tap used, swelling, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50492720 ↗InjuryAug 28, 2026Failure to Osseointegrate
Primary stability not achieved, no thread tap used, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50492711 ↗InjuryAug 28, 2026Failure to Osseointegrate
Implant didn't achieve osseointegration, implant wasn't completely covered with bone, no thread tap used, swelling, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50492665 ↗InjuryAug 28, 2026Failure to Osseointegrate
Implant didn't achieve osseointegration, implant wasn't completely covered with bone, no thread tap used, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50492627 ↗InjuryAug 28, 2026Loss of Osseointegration
Loss of osseointegration, implant wasn't completely covered with bone, no thread tap used, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50492561 ↗InjuryAug 28, 2026Failure to Osseointegrate
Primary stability not achieved, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50491710 ↗InjuryAug 28, 2026Failure to Osseointegrate
Implant didn't achieve osseointegration, implant wasn't completely covered with bone, no thread tap used, mobility.
Patient problems: Inadequate Osseointegration
MAUDE report 50491628 ↗InjuryJul 13, 2026Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, INADEQUATE BONE QUALITY/QUANTITY, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 25792670 ↗InjuryJun 12, 2026Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, IMMEDIATE IMPLANTATION, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 25482367 ↗InjuryJun 12, 2026Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, INFECTION (B)(6) ARE SAME PATIENT).
Patient problems: Inadequate Osseointegration
MAUDE report 25482342 ↗InjuryJun 12, 2026Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, INFECTION (B)(6) ARE SAME PATIENT).
Patient problems: Inadequate Osseointegration
MAUDE report 25482336 ↗InjuryJun 8, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, IMPLANT ACHIEVED OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, SMOKER, PERIODONTAL DISEASE, PERI-IMPLANTITIS.
Patient problems: Inadequate Osseointegration
MAUDE report 25425784 ↗InjuryJun 8, 2026Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, DIABETES MELLITUS, INFECTION, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 25425637 ↗InjuryJun 2, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, IMPLANT ACHIEVED OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, THREAD TAP USED, COMPROMISED IMMUNE RESISTANCE, PSYCHOLOGICAL DISORDER, DRUG OR ALCOHOL ABUSE, XEROSTOMIA, SMOKER, PERIODONTAL DISEASE, BONE RESORPTION, PAIN, MOBILITY (B)(6) ARE SAME PATIENT).
Patient problems: Inadequate Osseointegration
MAUDE report 25360973 ↗
Other Thommen Medical AG products
All Thommen Medical AG devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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