FDA Adverse Event Injury Summary report: N

TI TITAMAX IMPLANT (4.1)3.75X13

MDR report key: 7403400 · Received April 6, 2018

Report

Report Number
3008261720-2018-01584
Event Type
Injury
Date Received
April 6, 2018
Date of Event
March 6, 2018
Report Date
April 9, 2018
Manufacturer
NEODENT - JJGC S.A.
Product Code
DZE
UDI-DI
07898237566917
PMA / PMN Number
K101207
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
BR
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC. CONSIDERING THE SURGICAL METHODOLOGY, IT WAS SEEN THAT THE DENTIST HAS SELECTED AN IMPLANT DESIGN WHICH IS NOT RECOMMENDED FOR THE PATIENT'S BONE QUALITY.

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC. THE DENTIST SENT NEW INFORMATION ABOUT THE EVENT. THUS, THE EVENT EVALUATION WAS MODIFIED ACCORDING TO THE NEW INFORMATION RECEIVED. CONSIDERING THE SURGICAL METHODOLOGY, IT WAS SEEN THAT THE DENTIST HAS USED LESS DRILLS THAN RECOMMENDED TO PERFORM THE IMPLANT INSTALLATION.

Description of Event or Problem · 0

(B)(4) - THE DENTIST REPORTED THAT 3 MONTHS AFTER DENTAL IMPLANT WAS INSTALLED IN PATIENT¿S MOUTH, ITS NON-OSSEOINTEGRATION WAS OBSERVED. IN ADDITION, THE PROCEDURES OF IMMEDIATE LOAD WAS PERFORMED AND FENESTRATION OCCURRED DURING SURGERY.

Description of Event or Problem · 0

(B)(4). THE DENTIST REPORTED THAT 3 MONTHS AFTER DENTAL IMPLANT WAS INSTALLED IN PATIENT¿S MOUTH, ITS NON-OSSEOINTEGRATION WAS OBSERVED. IN ADDITION, THE PROCEDURES OF IMMEDIATE LOAD WAS PERFORMED AND FENESTRATION OCCURRED DURING SURGERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
245231 TI TITAMAX IMPLANT (4.1)3.75X13 ENDOSSEOUS DENTAL IMPLANT DZE NEODENT - JJGC S.A. 120723 07898237566917

Patients

Seq Age Sex Outcome Treatment
1 67 YR Required Intervention