NobelParallel S TiUltraRecalls & reported problems across all models
Nobel Biocare AB · 13 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 112
- Deaths reported
- 0
- Injuries reported
- 112
- Recalls
- 0
We found 13 models of NobelParallel S TiUltra by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 112 adverse event reports in the FDA's MAUDE database, received between Apr 18, 2026 and Sep 30, 2026 — classified as 112 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (99 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 NobelParallel S TiUltra problems
Device problems
- Failure to Osseointegrate99
- Osseointegration Problem8
- Migration3
- Loss of Osseointegration2
Patient problems
- No Clinical Signs, Symptoms or Conditions96
- Inflammation4
- Pain4
- Abscess2
- Fistula2
- Implant Pain2
- Sinus Perforation2
NobelParallel S TiUltra models
13 models, most reported first. Each model has its own page with its reports, recalls and device details.
- NobelParallel™ S TiUltra™ 302306Implant, endosseous, root-form25 reports
- NobelParallel™ S TiUltra™ 302307Implant, endosseous, root-form14 reports
- NobelParallel™ S TiUltra™ 302301Implant, endosseous, root-form12 reports
- NobelParallel™ S TiUltra™ 302309Implant, endosseous, root-form12 reports
- NobelParallel™ S TiUltra™ 302299Implant, endosseous, root-form11 reports
- NobelParallel™ S TiUltra™ 302305Implant, endosseous, root-form11 reports
- NobelParallel™ S TiUltra™ 302308Implant, endosseous, root-form6 reports
- NobelParallel™ S TiUltra™ 302316Implant, endosseous, root-form6 reports
- NobelParallel™ S TiUltra™ 302298Implant, endosseous, root-form5 reports
- NobelParallel™ S TiUltra™ 302315Implant, endosseous, root-form4 reports
- NobelParallel™ S TiUltra™ 302297Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUltra™ 302302Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUltra™ 302321Implant, endosseous, root-form2 reports
Recent NobelParallel S 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: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953657 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953653 ↗InjurySep 16, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795118 ↗InjurySep 16, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50795112 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781178 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781175 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781174 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781173 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781123 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781117 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781109 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781108 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781099 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50781098 ↗InjurySep 15, 2026Failure to Osseointegrate
Patient problems: Pain
MAUDE report 50781077 ↗
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
- NobelReplace Conical Connection TiUltra15 models · 31,165 reports
- NobelSpeedy88 models · 24,246 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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