meddevicedb.com FDA Device Reference

JDEvolution Plus L and JDEvolution Plus LE

K251148 Class II Traditional
Decision Date
2025-09-25
Sponsor / Applicant
Jdentalcare Srl

Technical Specification

510(k) Submission ID K251148
Product Code DZE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3640
Decision Date 2025-09-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

JDEvolution Plus L and JDEvolution Plus LE received FDA 510(k) clearance under submission number K251148, sponsored by Jdentalcare Srl. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-09-25.

Classification & Regulation

This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.