MAUDE Adverse Event Report: BICON, LLC INTEGRA-CP; DENTAL IMPLANT

Catalog Number	260-340-256
Medical Device Problem Code	Loss of Osseointegration (2408)
Health Effect - Clinical Code	Inadequate Osseointegration (2646)
Date of Event	03/02/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
According to the account, the patient is allergic to penicillin.There were many adjustments to the crown on #9 over the 2.5 years.Over time, bone loss and possible biomechanical overload had compromised the osseointegration as well as peri-implant infection at the implant site resulting in the removal of the implant.

• Brand Name: INTEGRA-CP
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): BICON, LLC; 501 arborway; boston MA 02130
• Manufacturer (Section G): BICON, LLC; 501 arborway; boston MA 02130
• Manufacturer Contact: richard wu ; 501 arborway; boston, MA 02130 ; 6175244443
• MDR Report Key: 24620081
• Report Number: 1223843-2026-00002
• Device Sequence Number: 10198930
• Product Code: DZE
• UDI-Device Identifier: 00813110022608
• UDI-Public: (01)00813110022608(17)280131(10)197241122B
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: K092035
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2023
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 03/17/2026

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 Catalogue Number: 260-340-256
• Device Lot Number: 197241122B
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/17/2026
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/17/2026
• Initial Report FDA Received Date: 03/17/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/17/2023
• 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: 56 YR
• Patient Sex: Male