NobelParallel S TiUniteRecalls & reported problems across all models
Nobel Biocare AB · 12 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 36
- Deaths reported
- 0
- Injuries reported
- 36
- Recalls
- 0
We found 12 models of NobelParallel S TiUnite by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 36 adverse event reports in the FDA's MAUDE database, received between May 7, 2026 and Sep 30, 2026 — classified as 36 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (26 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 TiUnite problems
Device problems
- Failure to Osseointegrate26
- Osseointegration Problem8
- Migration2
Patient problems
- No Clinical Signs, Symptoms or Conditions28
- Bone Fracture(s)4
- Unspecified Infection4
NobelParallel S TiUnite models
12 models, most reported first. Each model has its own page with its reports, recalls and device details.
- NobelParallel™ S TiUnite® 302375Implant, endosseous, root-form6 reports
- NobelParallel™ S TiUnite® 302370Implant, endosseous, root-form4 reports
- NobelParallel™ S TiUnite® 302376Implant, endosseous, root-form4 reports
- NobelParallel™ S TiUnite® 302377Implant, endosseous, root-form4 reports
- NobelParallel™ S TiUnite® 302383Implant, endosseous, root-form4 reports
- NobelParallel™ S TiUnite® 302368Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUnite® 302369Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUnite® 302371Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUnite® 302373Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUnite® 302374Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUnite® 302384Implant, endosseous, root-form2 reports
- NobelParallel™ S TiUnite® 302386Implant, endosseous, root-form2 reports
Recent NobelParallel S TiUnite 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 50953684 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953678 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953669 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953667 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953661 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953660 ↗InjurySep 8, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50678566 ↗InjurySep 8, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50678565 ↗InjurySep 8, 2026Migration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677955 ↗InjurySep 8, 2026Migration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50677954 ↗InjuryAug 6, 2026Osseointegration Problem
Lack of stability during placement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50167012 ↗InjuryAug 6, 2026Osseointegration Problem
Lack of stability during placement.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50167007 ↗InjuryAug 4, 2026Osseointegration Problem
InjuryAug 4, 2026Osseointegration Problem
InjuryAug 4, 2026Failure to Osseointegrate
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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