FDA Adverse Event Malfunction Summary report: N

BYTE RETAINER

MDR report key: 20091278 · Received August 28, 2024

Report

Report Number
3014845255-2024-00872
Event Type
Malfunction
Date Received
August 28, 2024
Report Date
October 7, 2025
Manufacturer
STRAIGHT SMILE, LLC
Product Code
KMY
UDI-DI
00850017524187
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

SINCE THIS EVENT RESULTED IN A SERIOUS INJURY, IT IS REPORTABLE PER 21 CFR PART 803.

Additional Manufacturer Narrative · 0

A DHR REVIEW WAS CONDUCTED WITH NO DISCREPANCIES NOTED.

Description of Event or Problem · 0

WHILE USING A BYTE RETAINERS, PATIENT REPORTED THAT THEIR RETAINERS ARE CUTTING INTO THEIR GUMS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1464427 BYTE RETAINER POSITIONER, TOOTH, PREFORMED KMY STRAIGHT SMILE, LLC 00850017524187

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention