NobelSpeedy® 32150 (UDI 07332747001518)Recalls & reported problems
Nobel Biocare AB · NobelSpeedy® Groovy RP 4.0x13mm · Class 2 · Implant
All models of NobelSpeedy (88)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Nobel Biocare NobelSpeedy dental implant is a root-form implant placed in the jawbone. The 1,483 reports most often describe the implant losing its bond with the jawbone, and patients mention implant failure, pain, infection and numbness. The reports list no deaths and 1,481 injuries. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 1,483
- Deaths reported
- 0
- Injuries reported
- 1,481
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,483 adverse event reports that list this exact device (DI 07332747001518), received between Sep 10, 2019 and Jun 12, 2026 — classified as 1,481 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Loss of Osseointegration” (1,114 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, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Loss of Osseointegration1,114
- Failure to Osseointegrate244
- Osseointegration Problem96
- Adverse Event Without Identified Device or Use Problem9
- Fracture6
- Premature Separation6
- Corroded2
- Insufficient Device Problem Information2
Patient problems
- Failure of Implant1,423
- Pain452
- Unspecified Infection210
- Numbness81
- No Clinical Signs, Symptoms or Conditions18
- Abscess6
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available6
- Sinus Perforation4
Recent adverse event reports
The 25 most recent of 1,483 reports, in the reporter's own words as published by the FDA.
InjuryJun 12, 2026Loss of Osseointegration
InjuryJun 12, 2026Loss of Osseointegration
InjuryApr 14, 2026Loss of Osseointegration
InjuryApr 14, 2026Loss of Osseointegration
InjuryApr 14, 2026Loss of Osseointegration
InjuryApr 14, 2026Loss of Osseointegration
InjuryApr 7, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24810154 ↗InjuryApr 7, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24810064 ↗InjuryApr 1, 2026Loss of Osseointegration
InjuryApr 1, 2026Loss of Osseointegration
InjuryMar 25, 2026Fracture
IMPLANT FRACTURE AT IMPLANT PLACEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24693610 ↗InjuryMar 25, 2026Fracture
IMPLANT FRACTURE AT IMPLANT PLACEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24693601 ↗InjuryFeb 16, 2026Loss of Osseointegration
InjuryFeb 16, 2026Loss of Osseointegration
InjuryFeb 16, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24350369 ↗InjuryFeb 16, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24350366 ↗InjuryJan 29, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24216441 ↗InjuryJan 29, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24216433 ↗InjuryJan 29, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24216413 ↗InjuryJan 29, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24216411 ↗InjuryJan 28, 2026Loss of Osseointegration
InjuryJan 28, 2026Loss of Osseointegration
InjuryJan 27, 2026Loss of Osseointegration
InjuryJan 27, 2026Loss of Osseointegration
InjuryOct 31, 2025Loss of Osseointegration; Loss of Osseointegration
Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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