MAUDE Adverse Event Report: DENTIUM USA IMPLANTIUM; DENTAL IMPLANT

Model Number	FX4808MLC
Medical Device Problem Codes	Failure to Osseointegrate (1863); Loss of Osseointegration (2408)
Health Effect - Clinical Codes	Failure of Implant (1924); Inadequate Osseointegration (2646)
Date of Event	08/24/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Please see attached summary memo.
Event or Problem Description
The doctor reported the implant was removed due to osseointegration failure 3 months after implant placement surgery.Bone quality around the area was type iii, and oral hygiene around the implant was good.The doctor reported no significant findings observed during the implant removal surgery.The patient has since recovered.
Additional Manufacturer Narrative
Please see attached summary memo.
Event or Problem Description
The doctor reported the implant was removed due to loss of osseointegration 3 years and 3 months after implant placement surgery.Bone quality around the area was type iii, and oral hygiene around the implant was good.The doctor reported no significant findings observed during the implant removal surgery.The patient has since recovered.
Event or Problem Description
The doctor reported the implant was removed due to loss of osseointegration 3 years and 3 months after implant placement surgery.Bone quality around the area was type iii, and oral hygiene around the implant was good.The doctor reported no significant findings observed during the implant removal surgery.The patient has since recovered.
Additional Manufacturer Narrative
Please see attached summary memo.

• Brand Name: IMPLANTIUM
• 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 son ; 6761 katella ave; cypress, CA 90630 ; 7142260229
• MDR Report Key: 15491505
• Report Number: 3005503242-2022-00098
• Device Sequence Number: 1856747
• Product Code: DZE
• UDI-Device Identifier: D755FX4808MLC0
• UDI-Public: D755FX4808MLC0
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K041368
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 09/26/2022

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: 04/25/2020
• Device Model Number: FX4808MLC
• Device Catalogue Number: FX4808MLC
• Device Lot Number: D23V06F22CS
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/16/2022
• Supplement Date Received by Manufacturer: 09/16/2022; 09/16/2022
• Initial Report FDA Received Date: 09/27/2022
• Supplement Report FDA Received Date: 10/04/2022; 10/05/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 04/26/2012
• 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: 76 YR
• Patient Sex: Female