FDA Adverse Event Injury Summary report: N

SMILEDIRECTCLUB ALIGNER SYSTEM

MDR report key: 12517286 · Received September 22, 2021

Report

Report Number
3014658399-2021-00086
Event Type
Injury
Date Received
September 22, 2021
Date of Event
August 30, 2021
Report Date
September 22, 2021
Manufacturer
ACCESS DENTAL LAB
Product Code
NXC
UDI-DI
00850007728038
PMA / PMN Number
K191990
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

BASED ON THE INFORMATION PROVIDED BY THE PATIENT AND INTERNAL INVESTIGATION CONDUCTED BY ACCESS DENTAL LAB, THERE IS NO CONCLUSIVE EVIDENCE THAT SUPPORTS OR OPPOSES THE FACT THAT THE ALIGNERS CAUSED, CONTRIBUTED, OR WOULD LIKELY CAUSE OR CONTRIBUTE TO THE REPORTED EVENT. THIS EVENT IS BEING FILED AS AN MDR SINCE THE PATIENT REPORTED SYMPTOMS OR PHYSIOLOGICAL CONDITIONS THAT DESCRIBE TOOTH FRACTURE (CRACKING).

Description of Event or Problem · 1

THE CUSTOMER REPORTED TEETH #18 AND 19 CRACKED WHILE WEARING ALIGNERS. A DENTIST EVALUATED THE CUSTOMER, BUT IT IS UNKNOWN IF MEDICAL INTERVENTION WAS REQUIRED. AS A RESULT, ALIGNER TREATMENT WAS DISCONTINUED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1408786 SMILEDIRECTCLUB ALIGNER SYSTEM SEQUENTIAL ALIGNER NXC ACCESS DENTAL LAB N/A N/A 00850007728038

Patients

Seq Age Sex Outcome Treatment
1 44 YR Other