MAUDE Adverse Event Report: NEODENT - JJGC S.A. GM TITAMAX ACQUA IMPLANT 3.75X8 MM; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	140.900
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Codes	Pain (1994); Tissue Damage (2104)
Date of Event	07/17/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The investigation of the complaint was carried out considering the analysis of the information given by the dentist in the guarantee form, visual conference of the product returned by the dentist and the evaluation of relevant production records.
Event or Problem Description
(b)(4).The dentist reported that 1 month and 10 days after the dental implant was installed in patient¿s mouth, its non- osseointegration was observed.

• Brand Name: GM TITAMAX ACQUA IMPLANT 3.75X8 MM
• 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: 8926524
• Report Number: 3008261720-2019-04278
• Device Sequence Number: 16216016
• Product Code: DZE
• UDI-Device Identifier: 07899878024637
• UDI-Public: 07899878024637
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• PMA/510(K) Number: K163194
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: distributor,foreign,health pr
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 08/23/2019
• Report Date (Section F): 07/31/2019

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: 07/29/2019
• Device Catalogue Number: 140.900
• Device Lot Number: 800311976
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/31/2019
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 08/23/2019
• Device Age: 24 MO
• Event Location: Other
• Date Report to Manufacturer: 07/31/2019
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/31/2019
• Initial Report FDA Received Date: 08/23/2019
• 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: 57 YR