MAUDE Adverse Event Report: NEODENT - JJGC S.A. CM TITAMAX IMPL TI 5.0X13; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	109.646
Medical Device Problem Codes	Failure to Osseointegrate (1863); Loss of Osseointegration (2408)
Health Effect - Clinical Code	Tissue Damage (2104)
Date of Event	04/24/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Exemption number: e2015015.
Event or Problem Description
The clinician reported that nearly 1 year and 3 months after the dental implant was placed in ada site 23 in the mouth, the implant had lost osseoointegration.The product will be forwarded to the manufacturer for investigation.There were no reported complications.
Additional Manufacturer Narrative
Exemption number: e2015015.After the evaluation, the event was considered as osseointegration failure.
Event or Problem Description
The clinician reported that nearly 1 year and 3 months after the dental implant was placed in ada site 23 in the mouth, the implant had lost osseointegration.The product will be forwarded to the manufacturer for investigation.There were no reported complications.(b)(4).

• Brand Name: CM TITAMAX IMPL TI 5.0X13
• Common Device Name: ENDOSSEOUS DENTAL IMPLANT
• Manufacturer (Section D): NEODENT - JJGC S.A.; av. juscelino kubitschek de; oliveira, 3291 cic; curitiba PR 81270 -200; BR 81270-200
• MDR Report Key: 7574684
• Report Number: 3008261720-2018-02497
• Device Sequence Number: 2073954
• Product Code: DZE
• UDI-Device Identifier: 07898237568942
• UDI-Public: 07898237568942
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K101945
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: distributor,foreign
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/06/2018
• Report Date (Section F): 05/09/2018

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: 03/31/2019
• Device Catalogue Number: 109.646
• Device Lot Number: 800124388
• Other Device ID Number: 07898237568942
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/19/2018
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 08/29/2018
• Device Age: 3 MO
• Event Location: Other
• Date Report to Manufacturer: 05/09/2018
• Initial Date Received by Manufacturer: 05/09/2018
• Supplement Date Received by Manufacturer: 07/19/2018
• Initial Report FDA Received Date: 06/06/2018
• Supplement Report FDA Received Date: 08/29/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 47 YR