FDA Adverse Event Injury Summary report: N

SCREW-VENT DENTAL IMPLANT

MDR report key: 24090 · Received December 23, 1994

Report

Report Number
2028280-1994-00603
Event Type
Injury
Date Received
December 23, 1994
Report Date
December 15, 1994
Manufacturer
CORE-VENT BBIO-ENGINEERING
Product Code
DZE
Product Problem
Yes
Report Source
Distributor report
Reporter Location
CA
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 DEENTAL IMPLANT DZE CORE-VENT BBIO-ENGINEERING SVA8 NI

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Required Intervention