Clearance Summary
GENIOVA aligners received FDA 510(k) clearance under submission number K233152, sponsored by Geniova Technologies Sociedad Limitada. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2024-12-12.
- Submission: K233152
- Applicant / Sponsor: Geniova Technologies Sociedad Limitada
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5470
- Decision date: 2024-12-12
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.