Clearance Summary
Neodent Implant System - Custom Abutments received FDA 510(k) clearance under submission number K250614, sponsored by Jjgc Indústria E Comércia DE Materiais Dentários S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-05-27.
- Submission: K250614
- Applicant / Sponsor: Jjgc Indústria E Comércia DE Materiais Dentários S.A.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3630
- Decision date: 2025-05-27
Classification & Regulation
This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.