TRICAM Dental Implant SystemRecalls & reported problems across all models
Ace Surgical Supply CO., Inc. · 16 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 950
- Deaths reported
- 0
- Injuries reported
- 950
- Recalls
- 0
We found 16 models of TRICAM Dental Implant System by Ace Surgical Supply CO., Inc. in the FDA's device registry (GUDID). Together they are named in 950 adverse event reports in the FDA's MAUDE database, received between Nov 24, 2015 and Jul 17, 2026 — classified as 950 injuries.
The most frequently reported specific device problem is “Osseointegration Problem” (709 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 TRICAM Dental Implant System problems
Device problems
- Osseointegration Problem709
- Failure to Osseointegrate559
- Insufficient Device Problem Information130
- Patient Device Interaction Problem17
- Loss of Osseointegration14
- Appropriate Device Problem Term/Code Not Available7
- Device Issue6
- Inadequacy of Device Shape and/or Size5
Patient problems
- Failure of Implant930
- Pain173
- Unspecified Infection93
- Swelling75
- Fistula53
- Numbness46
- Insufficient Information8
- Swelling/ Edema8
TRICAM Dental Implant System models
16 models, most reported first. Each model has its own page with its reports, recalls and device details.
- TRICAM Dental Implant System 304310IMPLANT, ENDOSSEOUS, ROOT-FORM143 reports
- TRICAM Dental Implant System 303510IMPLANT, ENDOSSEOUS, ROOT-FORM120 reports
- TRICAM Dental Implant System 304311IMPLANT, ENDOSSEOUS, ROOT-FORM98 reports
- TRICAM Dental Implant System 303511IMPLANT, ENDOSSEOUS, ROOT-FORM88 reports
- TRICAM Dental Implant System 305010IMPLANT, ENDOSSEOUS, ROOT-FORM84 reports
- TRICAM Dental Implant System 303513IMPLANT, ENDOSSEOUS, ROOT-FORM82 reports
- TRICAM Dental Implant System 304313IMPLANT, ENDOSSEOUS, ROOT-FORM80 reports
- TRICAM Dental Implant System 304308IMPLANT, ENDOSSEOUS, ROOT-FORM74 reports
- TRICAM Dental Implant System 303508IMPLANT, ENDOSSEOUS, ROOT-FORM55 reports
- TRICAM Dental Implant System 305008IMPLANT, ENDOSSEOUS, ROOT-FORM46 reports
- TRICAM Dental Implant System 305011IMPLANT, ENDOSSEOUS, ROOT-FORM27 reports
- TRICAM Dental Implant System 305013IMPLANT, ENDOSSEOUS, ROOT-FORM23 reports
- TRICAM Dental Implant System 303516IMPLANT, ENDOSSEOUS, ROOT-FORM15 reports
- TRICAM Dental Implant System 304316IMPLANT, ENDOSSEOUS, ROOT-FORM10 reports
- TRICAM Dental Implant System 305016IMPLANT, ENDOSSEOUS, ROOT-FORM4 reports
- TRICAM Dental Implant System 30250604ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 report
Recent TRICAM Dental Implant System adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJul 17, 2026Failure to Osseointegrate
InjuryJul 17, 2026Failure to Osseointegrate
InjuryJul 17, 2026Failure to Osseointegrate
InjuryJul 17, 2026Failure to Osseointegrate
InjuryMay 18, 2026Failure to Osseointegrate
InjuryMay 18, 2026Failure to Osseointegrate
InjuryMay 18, 2026Failure to Osseointegrate
InjuryMay 18, 2026Failure to Osseointegrate
InjuryJun 27, 2025Loss of Osseointegration; Loss of Osseointegration
PT COMPLAINED OF PAIN WHILE EATING. IMPLANT FOUND TO BE MOBILE.
Patient problems: Failure of Implant
MAUDE report 22344518 ↗InjurySep 30, 2024Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
InjurySep 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjurySep 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT FAILED THE DAY OF IMPRESSIONS FOR CROWN.
Patient problems: Failure of Implant
MAUDE report 20334171 ↗InjurySep 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT FELL OUT OF THE MOUTH AFTER 2 WEEKS.
Patient problems: Failure of Implant
MAUDE report 20334070 ↗InjurySep 30, 2024Failure to Osseointegrate; Failure to Osseointegrate
InjuryAug 7, 2024Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
Other Ace Surgical Supply CO., Inc. products
All Ace Surgical Supply CO., Inc. 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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