SPI CONTACTRecalls & reported problems across all models
Thommen Medical AG · 18 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 217
- Deaths reported
- 0
- Injuries reported
- 217
- Recalls
- 0
We found 18 models of SPI CONTACT by Thommen Medical AG in the FDA's device registry (GUDID). Together they are named in 217 adverse event reports in the FDA's MAUDE database, received between Apr 27, 2018 and Jun 23, 2026 — classified as 217 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (151 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 problems
Device problems
- Failure to Osseointegrate151
- Loss of Osseointegration61
- Break4
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Inadequate Osseointegration124
- No Code Available90
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available3
SPI CONTACT models
18 models, most reported first. Each model has its own page with its reports, recalls and device details.
- SPI CONTACT 4.13.214Implant, Endosseous, Root-Form65 reports
- SPI CONTACT 4.13.224Implant, Endosseous, Root-Form32 reports
- SPI CONTACT 4.13.211Implant, Endosseous, Root-Form29 reports
- SPI CONTACT 4.13.221Implant, Endosseous, Root-Form22 reports
- SPI CONTACT 4.13.220Implant, Endosseous, Root-Form14 reports
- SPI CONTACT 4.13.234Implant, Endosseous, Root-Form9 reports
- SPI CONTACT 4.13.231Implant, Endosseous, Root-Form7 reports
- SPI CONTACT 4.13.230Implant, Endosseous, Root-Form7 reports
- SPI CONTACT 4.13.213Implant, Endosseous, Root-Form7 reports
- SPI CONTACT 4.13.232Implant, Endosseous, Root-Form5 reports
- SPI CONTACT 4.13.222Implant, Endosseous, Root-Form5 reports
- SPI CONTACT 4.13.212Implant, Endosseous, Root-Form5 reports
- SPI CONTACT 4.13.244Implant, Endosseous, Root-Form3 reports
- SPI CONTACT 4.13.233Implant, Endosseous, Root-Form2 reports
- SPI CONTACT 4.13.223Implant, Endosseous, Root-Form2 reports
- SPI CONTACT 4.13.242Implant, Endosseous, Root-Form1 report
- SPI CONTACT 4.13.241Implant, Endosseous, Root-Form1 report
- SPI CONTACT 4.13.240Implant, Endosseous, Root-Form1 report
Recent SPI CONTACT adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJun 23, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, SMOKER, PAIN.
Patient problems: Inadequate Osseointegration
MAUDE report 25591087 ↗InjuryApr 13, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, IMPLANT ACHIEVED OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, PERIODONTAL DISEASE, PERI-IMPLANTITIS, MOBILITY (B)(6) ARE SAME PATIENT).
Patient problems: Inadequate Osseointegration
MAUDE report 24854840 ↗InjuryMay 9, 2025Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, PERI-IMPLANTITIS, MOBILITY ((B)(6) ARE SAME PATIENT).
Patient problems: Inadequate Osseointegration
MAUDE report 21992009 ↗InjuryOct 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, SMOKER, LOCAL INFECTION / SUBACUTE CHRONIC OSTEITIS, PERI-IMPLANTITIS, INFECTION
Patient problems: Inadequate Osseointegration
MAUDE report 20543650 ↗InjuryOct 24, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, LOCAL INFECTION / SUBACUTE CHRONIC OSTEITIS, IMMEDIATE IMPLANTATION, MOBILITY
Patient problems: Inadequate Osseointegration
MAUDE report 20521016 ↗InjuryOct 23, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PAIN
Patient problems: Inadequate Osseointegration
MAUDE report 20512503 ↗InjuryOct 23, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, OVERHEATING OF BONE, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 20512479 ↗InjurySep 6, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, PRECEDING/SIMULTANEOUS BONE AUGMENTATION, INFECTION, ABSCESS.
Patient problems: Inadequate Osseointegration
MAUDE report 20155009 ↗InjuryAug 7, 2024Failure to Osseointegrate; Failure to Osseointegrate
PRIMARY STABILITY NOT ACHIEVED, THREAD TAP USED, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 19927940 ↗InjuryJul 16, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT DIDN'T ACHIEVE OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, SMOKER, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 19747973 ↗InjuryJun 5, 2024Loss of Osseointegration; Loss of Osseointegration
LOSS OF OSSEOINTEGRATION, PRIMARY STABILITY WAS ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED.
Patient problems: Inadequate Osseointegration
MAUDE report 19465520 ↗InjuryMay 7, 2024Failure to Osseointegrate; Failure to Osseointegrate
PRIMARY STABILITY NOT ACHIEVED, IMPLANT WASN'T COMPLETELY COVERED WITH BONE, NO THREAD TAP USED, INADEQUATE BONE QUALITY/QUANTITY, MOBILITY.
Patient problems: Inadequate Osseointegration
MAUDE report 19257217 ↗InjuryMay 7, 2024Failure to Osseointegrate; Failure to Osseointegrate
PRIMARY STABILITY NOT ACHIEVED, IMPLANT WAS COMPLETELY COVERED WITH BONE, NO THREAD TAP USED.
Patient problems: Inadequate Osseointegration
MAUDE report 19257165 ↗InjuryMar 26, 2024Failure to Osseointegrate; Failure to Osseointegrate
PRIMARY STABILITY NOT ACHIEVED, IMPLANT WASN'T COMPLETELY COVERED WITH BONE, THREAD TAP USED, SMOKER, PERIODONTAL DISEASE, INADEQUATE BONE QUALITY/QUANTITY.
Patient problems: Inadequate Osseointegration
MAUDE report 18976961 ↗InjuryFeb 28, 2024Failure to Osseointegrate; Failure to Osseointegrate
PRIMARY STABILITY NOT ACHIEVED, IMPLANT WASN'T COMPLETELY COVERED WITH BONE, THREAD TAP USED, SMOKER, PERIODONTAL DISEASE, INADEQUATE BONE QUALITY/QUANTITY.
Patient problems: Inadequate Osseointegration
MAUDE report 18795350 ↗
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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