FDA Adverse Event Injury Summary report: N

OSSEOSPEED 4.5 - 11 MM(IMPLANTS)

MDR report key: 11934663 · Received June 3, 2021

Report

Report Number
9612468-2021-29912
Event Type
Injury
Date Received
June 3, 2021
Date of Event
July 18, 2019
Report Date
May 13, 2021
Manufacturer
DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB)
Product Code
DZE
PMA / PMN Number
K091239
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
DENTIST

Narratives

Additional Manufacturer Narrative · 1

THEREFORE, BECAUSE A SERIOUS INJURY RESULTED, THIS EVENT IS REPORTABLE PER 21 CFR PART 803.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT EXPERIENCED A DENTAL IMPLANT LOSS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
826629 OSSEOSPEED 4.5 - 11 MM(IMPLANTS) IMPLANT, ENDOSSEOUS, ROOT-FORM DZE DENTSPLY IMPLANTS (A DIVISION OF DENTSPLY IH AB) NA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention