MAUDE Adverse Event Report: NEODENT - JJGC S.A. TI TITAMAX IMPLANT (5.0) 5.0X13 MM; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	109.297
Medical Device Problem Code	Loss of Osseointegration (2408)
Health Effect - Clinical Codes	Unspecified Infection (1930); Pain (1994); Tissue Damage (2104)
Date of Event	05/16/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The lot number reported by the dentist was not verified by the crm system, so it was not considered.The information provided in this report was based on information given by the dentist in neodent¿s products warranty form that was recorded in the system and is used by both the manufacturer and the subsidiary.The original complaint and the product were received by the subsidiary and did not arrive in the manufacturer yet.When this happens, a new evaluation of the complaint will be carried out and, if necessary, a new follow-up report will be send.
Event or Problem Description
(b)(4) - the dentist reported that 2 years and 2 months after the dental implant was installed in intraoral region 13#, its loss of osseointegration was observed.Moreover, the patient presented bone type ii.

• Brand Name: TI TITAMAX IMPLANT (5.0) 5.0X13 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: 9122553
• Report Number: 3008261720-2019-04821
• Device Sequence Number: 11397425
• Product Code: DZE
• UDI-Device Identifier: 07898237566979
• UDI-Public: 07898237566979
• Combination Product (Y/N): N
• Initial Reporter Country: ES
• PMA/510(K) Number: K101207
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• 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): 09/26/2019
• Report Date (Section F): 09/01/2019

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 Catalogue Number: 109.297
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 09/26/2019
• Event Location: Other
• Date Report to Manufacturer: 09/01/2019
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/01/2019
• Initial Report FDA Received Date: 09/26/2019
• 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