MAUDE Adverse Event Report: DENTIUM USA NRLINE; DENTAL IMPLANT

Model Number	GFX3011S
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Codes	Failure of Implant (1924); Unspecified Infection (1930); Inadequate Osseointegration (2646)
Date of Event	10/27/2023
Type of Reportable Event	Serious Injury
Event or Problem Description
The doctor reported the implant was removed due to implant fracture approximately 1 year and 5 months after implant placement.Bone quality around the area was type iii, and oral hygiene around the implant was moderate.Local infection and peri-implantitis were observed during the implant removal surgery.Bone augmentation material was used in implant placement surgery.Trauma history related to implant fracture was reported.The patient has recovered but will need another surgical intervention.

• Brand Name: NRLINE
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): DENTIUM USA; 6761 katella ave; cypress CA 90630
• Manufacturer (Section G): DENTIUM USA; 6761 katella ave; cypress CA 90630
• Manufacturer Contact: eun kyung son ; 6761 katella ave; cypress, CA 90630 ; 7142260029
• MDR Report Key: 18242868
• Report Number: 3005503242-2023-00141
• Device Sequence Number: 7116145
• Product Code: DZE
• UDI-Device Identifier: 08809460302356
• UDI-Public: 08809460302356
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K153268
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 11/30/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 09/13/2024
• Device Model Number: GFX3011S
• Device Lot Number: 201609090037
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/27/2023
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 11/30/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/14/2016
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 75 YR
• Patient Sex: Female