Clearance Summary
Guided Bone Regeneration System received FDA 510(k) clearance under submission number K254286, sponsored by DentalMaster(Xiamen)Medical Technology Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-08-24.
- Submission: K254286
- Applicant / Sponsor: DentalMaster(Xiamen)Medical Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.4880
- Decision date: 2026-08-24
Classification & Regulation
This clearance is catalogued under FDA product code DZL and 21 CFR 872.4880, within the Dental review panel as a Class II device.