meddevicedb.com FDA Device Reference

Integrated Endo System (Meet Endo-II)

K242317 Class II Traditional
Decision Date
2025-02-13
Sponsor / Applicant
Denjoy Dental Co., Ltd.

Technical Specification

510(k) Submission ID K242317
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2025-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Integrated Endo System (Meet Endo-II) received FDA 510(k) clearance under submission number K242317, sponsored by Denjoy Dental 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 2025-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.