NobelActive S TiUltraRecalls & reported problems across all models
Nobel Biocare AB · 16 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 163
- Deaths reported
- 0
- Injuries reported
- 163
- Recalls
- 0
We found 16 models of NobelActive S TiUltra by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 163 adverse event reports in the FDA's MAUDE database, received between Apr 15, 2026 and Sep 29, 2026 — classified as 163 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (114 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 NobelActive S TiUltra problems
Device problems
- Failure to Osseointegrate114
- Osseointegration Problem39
- Loss of Osseointegration8
- Migration2
Patient problems
- No Clinical Signs, Symptoms or Conditions135
- Unspecified Infection10
- Fistula6
- Abscess2
- Aspiration/Inhalation2
- Bone Fracture(s)2
- Implant Pain2
- Inflammation2
NobelActive S TiUltra models
16 models, most reported first. Each model has its own page with its reports, recalls and device details.
- NobelActive® S TiUltra™ 302276Implant, endosseous, root-form24 reports
- NobelActive® S TiUltra™ 302280Implant, endosseous, root-form22 reports
- NobelActive® S TiUltra™ 302281Implant, endosseous, root-form16 reports
- NobelActive® S TiUltra™ 302275Implant, endosseous, root-form12 reports
- NobelActive® S TiUltra™ 302277Implant, endosseous, root-form12 reports
- NobelActive® S TiUltra™ 302285Implant, endosseous, root-form12 reports
- NobelActive® S TiUltra™ 302287Implant, endosseous, root-form12 reports
- NobelActive® S TiUltra™ 302274Implant, endosseous, root-form10 reports
- NobelActive® S TiUltra™ 302282Implant, endosseous, root-form10 reports
- NobelActive® S TiUltra™ 302286Implant, endosseous, root-form10 reports
- NobelActive® S TiUltra™ 302279Implant, endosseous, root-form8 reports
- NobelActive® S TiUltra™ 302273Implant, endosseous, root-form6 reports
- NobelActive® S TiUltra™ 302295Implant, endosseous, root-form3 reports
- NobelActive® S TiUltra™ 302284Implant, endosseous, root-form2 reports
- NobelActive® S TiUltra™ 302288Implant, endosseous, root-form2 reports
- NobelActive® S TiUltra™ 302294Implant, endosseous, root-form2 reports
Recent NobelActive 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 29, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940410 ↗InjurySep 29, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940406 ↗InjurySep 29, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940400 ↗InjurySep 29, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940396 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50925424 ↗InjurySep 28, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50925422 ↗InjurySep 20, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50834861 ↗InjurySep 20, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50834856 ↗InjurySep 19, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833634 ↗InjurySep 19, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833632 ↗InjurySep 19, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833271 ↗InjurySep 19, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833269 ↗InjurySep 19, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833256 ↗InjurySep 19, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833253 ↗InjurySep 19, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833211 ↗
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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