Clearance Summary
Endo Motor received FDA 510(k) clearance under submission number K220829, sponsored by Foshan Coxo Medical Instrument 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 2023-05-18.
- Submission: K220829
- Applicant / Sponsor: Foshan Coxo Medical Instrument Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.4200
- Decision date: 2023-05-18
Classification & Regulation
This clearance is catalogued under FDA product code EKX and 21 CFR 872.4200, within the Dental review panel as a Class I device.