NobelReplace Conical Connection TiUltraRecalls & reported problems across all models
Nobel Biocare AB · 15 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 31,165
- Deaths reported
- 0
- Injuries reported
- 30,836
- Recalls
- 0
We found 15 models of NobelReplace Conical Connection TiUltra by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 31,165 adverse event reports in the FDA's MAUDE database, received between Oct 29, 2021 and Sep 30, 2026 — classified as 30,836 injuries, 329 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (23,391 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 NobelReplace Conical Connection TiUltra problems
Device problems
- Failure to Osseointegrate23,391
- Loss of Osseointegration3,664
- Osseointegration Problem1,939
- Adverse Event Without Identified Device or Use Problem581
- Patient Device Interaction Problem491
- Fracture263
- Migration173
- Difficult to Insert168
Patient problems
- Failure of Implant20,425
- No Clinical Signs, Symptoms or Conditions8,326
- Unspecified Infection2,419
- Pain1,663
- Abscess355
- Inflammation344
- Numbness263
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available259
NobelReplace Conical Connection TiUltra models
15 models, most reported first. Each model has its own page with its reports, recalls and device details.
- NobelReplace® Conical Connection TiUltra™ 300343IMPLANT, ENDOSSEOUS, ROOT-FORM5,787 reports
- NobelReplace® Conical Connection TiUltra™ 300338IMPLANT, ENDOSSEOUS, ROOT-FORM4,099 reports
- NobelReplace® Conical Connection TiUltra™ 300348IMPLANT, ENDOSSEOUS, ROOT-FORM3,289 reports
- NobelReplace® Conical Connection TiUltra™ 300342IMPLANT, ENDOSSEOUS, ROOT-FORM3,124 reports
- NobelReplace® Conical Connection TiUltra™ 300339IMPLANT, ENDOSSEOUS, ROOT-FORM2,896 reports
- NobelReplace® Conical Connection TiUltra™ 300344IMPLANT, ENDOSSEOUS, ROOT-FORM2,629 reports
- NobelReplace® Conical Connection TiUltra™ 300347IMPLANT, ENDOSSEOUS, ROOT-FORM2,248 reports
- NobelReplace® Conical Connection TiUltra™ 300340IMPLANT, ENDOSSEOUS, ROOT-FORM1,828 reports
- NobelReplace® Conical Connection TiUltra™ 300345IMPLANT, ENDOSSEOUS, ROOT-FORM1,607 reports
- NobelReplace® Conical Connection TiUltra™ 300337IMPLANT, ENDOSSEOUS, ROOT-FORM1,513 reports
- NobelReplace® Conical Connection TiUltra™ 300349IMPLANT, ENDOSSEOUS, ROOT-FORM930 reports
- NobelReplace® Conical Connection TiUltra™ 300350IMPLANT, ENDOSSEOUS, ROOT-FORM429 reports
- NobelReplace® Conical Connection TiUltra™ 300346IMPLANT, ENDOSSEOUS, ROOT-FORM360 reports
- NobelReplace® Conical Connection TiUltra™ 300341IMPLANT, ENDOSSEOUS, ROOT-FORM336 reports
- NobelReplace® Conical Connection TiUltra™ 300351IMPLANT, ENDOSSEOUS, ROOT-FORM90 reports
Recent NobelReplace Conical Connection TiUltra adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Failure to Osseointegrate
Patient problems: Abscess
MAUDE report 50954531 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: Abscess
MAUDE report 50954530 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954486 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954479 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954441 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954436 ↗InjurySep 30, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954410 ↗InjurySep 30, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954408 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954204 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954201 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954188 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954184 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954183 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954179 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954157 ↗
Other Nobel Biocare AB products
- NobelActive56 models · 152,066 reports
- NobelReplace120 models · 138,221 reports · 15 recalls
- NobelParallel54 models · 132,525 reports
- NobelActive TiUltra28 models · 82,969 reports
- NobelParallel Conical Connection TiUltra27 models · 68,868 reports
- Replace Select107 models · 33,616 reports
- NobelSpeedy88 models · 24,246 reports
- Brånemark System141 models · 19,899 reports
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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