MyClearALIGN Dental Aligner System— 510(k) K221475
Substantially EquivalentKey Dental Technologies, LLC
FDA 510(k) clearance K221475 for MyClearALIGN Dental Aligner System, Substantially Equivalent on 2022-08-31. Applicant: Key Dental Technologies, LLC.
Clearance details
- Applicant
- Key Dental Technologies, LLC
- Product code
- Code NXC
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chapel Hill, NC, 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.