NobelParallel™ 37972 (UDI 07332747091519)Recalls & reported problems

Nobel Biocare AB · NobelParallel™ Conical Connection RP 4.3x10mm · Class 2 · Implant

Quick summary

This NobelParallel dental implant is a root-form implant placed in the jawbone. Its 3,168 reports mostly describe the implant failing to fuse with the jawbone, with some implants breaking and patients reporting pain, infection and numbness. The reports include no deaths and 3,163 injuries. No recalls name this device. Reports were lower in the most recent year (117) than in the year before (163).

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: 3,175
Deaths reported: 0
Injuries reported: 3,170
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 3,175 adverse event reports that list this exact device (DI 07332747091519), received between Jul 31, 2019 and Sep 18, 2026 — classified as 3,170 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (1,500 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

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Failure to Osseointegrate1,500
Loss of Osseointegration1,425
Fracture118
Osseointegration Problem97
Adverse Event Without Identified Device or Use Problem15
Material Deformation9
Malposition of Device7
Migration4

Patient problems

Failure of Implant2,947
Pain485
Unspecified Infection215
No Clinical Signs, Symptoms or Conditions163
Numbness76
Abscess9
Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available8
Implant Pain8

Recent adverse event reports

The 25 most recent of 3,175 reports, in the reporter's own words as published by the FDA.

InjurySep 18, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50830804 ↗
InjurySep 18, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50830801 ↗
InjurySep 18, 2026Loss of Osseointegration
Patient problems: Implant Pain
MAUDE report 50830474 ↗
InjurySep 18, 2026Loss of Osseointegration
Patient problems: Implant Pain
MAUDE report 50830472 ↗
InjurySep 9, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50701317 ↗
InjurySep 9, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50701316 ↗
InjuryAug 26, 2026Failure to Osseointegrate
Failure to osseointegrate.
Patient problems: Unspecified Infection
MAUDE report 50463792 ↗
InjuryAug 26, 2026Failure to Osseointegrate
Failure to Osseo integrate.
Patient problems: Unspecified Infection
MAUDE report 50463784 ↗
InjuryAug 22, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50392960 ↗
InjuryAug 4, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50135183 ↗
InjuryAug 4, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50135166 ↗
InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50030547 ↗
InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50030546 ↗
InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50001937 ↗
InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50001936 ↗
InjuryJul 17, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25863436 ↗
InjuryJul 17, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25863429 ↗
InjuryJul 8, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25755785 ↗
InjuryJul 8, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25755783 ↗
InjuryJul 8, 2026Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25754821 ↗
InjuryJul 8, 2026Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25754814 ↗
InjuryJul 7, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25740911 ↗
InjuryJul 7, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25740910 ↗
InjuryJun 30, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25672106 ↗
InjuryJun 30, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25672095 ↗

Device details

UDI-DI	`07332747091519`
Brand	NobelParallel™
Model	37972
Company	Nobel Biocare AB
Product code	DZE · IMPLANT, ENDOSSEOUS, ROOT-FORM
Class	Class 2
FDA submission	None listed
Implant	Yes
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	Not in Commercial Distribution
Record updated	Oct 12, 2023

Device type (GMDN): Screw endosteal dental implant, two-piece

A sterile device made of alloplastic materials [e.g., titanium (Ti), stainless steel, ceramic] intended to be surgically implanted into alveolar and/or basal bone of the mandible or maxilla to provide support and a means of retention for a dental prosthesis (e.g., bridge, single-tooth, overdenture). It is a two-piece device composed of an anchorage component (implant body) in the form of a threaded screw that is implanted into bone, and a retention component (implant abutment), typically attached to the anchorage component after implantation, that protrudes through gingival tissues to support the prosthesis.

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.