3M Clarity Aligners— 510(k) K192119
Substantially Equivalent3M Company
FDA 510(k) clearance K192119 for 3M Clarity Aligners, Substantially Equivalent on 2019-09-05. Applicant: 3M Company.
Clearance details
- Applicant
- 3M Company
- Product code
- Code NXC
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Saint Paul, MN, US
Adverse events under product code NXC
product code NXC- Injury
- 15,206
- Malfunction
- 2,576
- Other
- 9
- Total
- 17,791
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.