FDA Adverse Event
Injury
Summary report: N
BYTE RETAINER
MDR report key: 20262316
·
Received September 19, 2024
Report
- Report Number
- 3014845255-2024-01105
- Event Type
- Injury
- Date Received
- September 19, 2024
- Report Date
- November 24, 2025
- Manufacturer
- STRAIGHT SMILE, LLC
- Product Code
- KMY
- UDI-DI
- 00850017524187
- Adverse Event
- 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 #7 AND #8 TEETH WERE CHIPPED AND HAD TO BE REPAIRED BY THEIR DENTIST. THEIR RETAINER NOW DOES NOT FIT. PROVIDED TIPS FOR DISCOMFORT AND SOAKING AND ASKED TO FOLLOW UP.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2296523 | BYTE RETAINER | POSITIONER, TOOTH, PREFORMED | KMY | STRAIGHT SMILE, LLC | BYTERETAINER | 00850017524187 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Required Intervention |