FDA Adverse Event Injury Summary report: N

SCREW-VENT DENTAL IMPLANT

MDR report key: 14051 · Received May 2, 1994

Report

Report Number
2028280-1994-00237
Event Type
Injury
Date Received
May 2, 1994
Date of Event
April 21, 1994
Report Date
April 21, 1994
Manufacturer
CORE-VENT BIO ENGINEERING
Product Code
DZE
Product Problem
Yes
Report Source
Distributor report
Reporter Location
WI, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

DENTAL IMPLANAT FAILED TO OSSEOINTEGRATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SCREW-VENT DENTAL IMPLANT ENDOSTEAL DENTAL IMPLANT DZE CORE-VENT BIO ENGINEERING SVA8

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Required Intervention