FDA Adverse Event Injury Summary report: N

SYBRONPRO TL

MDR report key: 1664280 · Received April 21, 2010

Report

Report Number
2016150-2010-00055
Event Type
Injury
Date Received
April 21, 2010
Date of Event
February 23, 2010
Report Date
March 22, 2010
Manufacturer
EBI INC.
Product Code
DZE
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
SC, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

ON MARCH 22, 2010, A DOCTOR REPORTED THAT A PATIENT LOST A DENTAL IMPLANT SEVEN MONTHS AFTER PLACEMENT DUE UNKNOWN REASONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SYBRONPRO TL IMPLANT, ENDOSSEOUS, ROOT-FORM DZE EBI INC. 081073

Patients

Seq Age Sex Outcome Treatment
1 68 YR Other| R