MAUDE Adverse Event Report: NEODENT - JJGC S.A. TITAMAX SMART IMPLANT (4.1) 3.75X13; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	109.152
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Codes	Pain (1994); Tissue Damage (2104)
Date of Event	02/01/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The installation and removal date were disconsidered because the removal date was anterior to the installation date.The information provided in this report was based on information given by the dentist in neodent¿s products warranty form.The original complaint was 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 follow-up report will be send.
Event or Problem Description
(b)(4).The dentist reported that 1 months and 15 days after the dental implant was installed in patient¿s mouth, its non- osseointegration was observed.Moreover, the patient presented bone type ii.
Additional Manufacturer Narrative
The installation and removal date were disconsidered because the removal date was anterior to the installation date.Follow-up being sent to include information about patient's conditions.
Event or Problem Description
(b)(4) - the dentist reported that 1 months and 15 days after the dental implant was installed in patient¿s mouth, its non- osseointegration was observed.Moreover, the patient presented bone type ii.

• Brand Name: TITAMAX SMART IMPLANT (4.1) 3.75X13
• 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: 8811774
• Report Number: 3008261720-2019-03770
• Device Sequence Number: 2657599
• Product Code: DZE
• UDI-Device Identifier: 07898237566726
• UDI-Public: 07898237566726
• Combination Product (Y/N): N
• Initial Reporter Country: ES
• PMA/510(K) Number: K133510
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor,foreign,health pr
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup
• Report Date (Section B): 07/22/2019
• Report Date (Section F): 06/21/2019

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: 12/03/2018
• Device Catalogue Number: 109.152
• Device Lot Number: 800112918
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 08/21/2019
• Device Age: 50 MO
• Event Location: Other
• Date Report to Manufacturer: 06/21/2019
• Initial Date Received by Manufacturer: 06/21/2019
• Supplement Date Received by Manufacturer: 06/21/2019
• Initial Report FDA Received Date: 07/22/2019
• Supplement Report FDA Received Date: 08/21/2019
• 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