NobelParallel™ 37973 (UDI 07332747091526)Recalls & reported problems
Nobel Biocare AB · NobelParallel™ Conical Connection RP 4.3x11.5mm · Class 2 · Implant
Quick summary
This Nobel Biocare NobelParallel Conical Connection dental implant has 2,510 adverse event reports, with no deaths and 2,501 injuries. Most reports describe the implant failing to bond with the jawbone or losing that bond later, with patients reporting implant failure, pain and infection. Reports fell to 99 in the last 12 months from 157 in the 12 months before. 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
- 2,518
- Deaths reported
- 0
- Injuries reported
- 2,509
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2,518 adverse event reports that list this exact device (DI 07332747091526), received between Sep 10, 2019 and Sep 30, 2026 — classified as 2,509 injuries, 9 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (1,258 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate1,258
- Loss of Osseointegration1,052
- Osseointegration Problem89
- Fracture70
- Adverse Event Without Identified Device or Use Problem27
- Insufficient Device Problem Information5
- Malposition of Device4
- Migration4
Patient problems
- Failure of Implant2,329
- Pain359
- Unspecified Infection166
- No Clinical Signs, Symptoms or Conditions118
- Numbness62
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available12
- Inflammation12
- Abscess7
Recent adverse event reports
The 25 most recent of 2,518 reports, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Loss of Osseointegration
Patient problems: Pain
MAUDE report 50953546 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Pain
MAUDE report 50953542 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50743143 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50743140 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50701469 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50701464 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50701463 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50701462 ↗InjuryAug 26, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50463757 ↗InjuryAug 26, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50463753 ↗InjuryAug 11, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50214947 ↗InjuryAug 11, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50214942 ↗InjuryJul 29, 2026Loss of Osseointegration
InjuryJul 15, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25832562 ↗InjuryJul 15, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25832459 ↗InjuryJul 8, 2026Loss of Osseointegration
InjuryJul 8, 2026Loss of Osseointegration
InjuryJun 25, 2026Loss of Osseointegration
InjuryJun 25, 2026Loss of Osseointegration
InjuryJun 11, 2026Fracture
COMPONENT FRACTURED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25479491 ↗InjuryJun 11, 2026Fracture
COMPONENT FRACTURED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25479472 ↗InjuryJun 4, 2026Loss of Osseointegration
InjuryJun 4, 2026Loss of Osseointegration
InjuryJun 3, 2026Loss of Osseointegration
InjuryJun 3, 2026Loss of Osseointegration
Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.