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Dentis s-Clean Abutment Mini

K220440 Class II Traditional
Decision Date
2022-06-16
Sponsor / Applicant
Dentis Co., Ltd.

Technical Specification

510(k) Submission ID K220440
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2022-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dentis s-Clean Abutment Mini received FDA 510(k) clearance under submission number K220440, sponsored by Dentis 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 2022-06-16.

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.