Clearance Summary
Customized Abutment and Screw received FDA 510(k) clearance under submission number K242768, sponsored by Chengdu Besmile Medical Technology Co., Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-09-02.
- Submission: K242768
- Applicant / Sponsor: Chengdu Besmile Medical Technology Co., Ltd.
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3630
- Decision date: 2025-09-02
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.