meddevicedb.com FDA Device Reference

ChecQ (AC100)

K241065 Class I Traditional
Decision Date
2025-03-21
Sponsor / Applicant
Dentis Co., Ltd.

Technical Specification

510(k) Submission ID K241065
Product Code EKX
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2025-03-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ChecQ (AC100) received FDA 510(k) clearance under submission number K241065, 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 2025-03-21.

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.