Clearance Summary
Vivid Aligners received FDA 510(k) clearance under submission number K190003, sponsored by Orthodent Laboratory, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-11-06.
- Submission: K190003
- Applicant / Sponsor: Orthodent Laboratory, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5470
- Decision date: 2019-11-06
Classification & Regulation
This clearance is catalogued under FDA product code NXC and 21 CFR 872.5470, within the Dental review panel as a Class II device.