meddevicedb.com FDA Device Reference

SmartLite Pro Modular LED Curing Light

K191865 Class II Traditional
Decision Date
2019-11-20
Sponsor / Applicant
Dentsply Sirona

Technical Specification

510(k) Submission ID K191865
Product Code EBZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6070
Decision Date 2019-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmartLite Pro Modular LED Curing Light received FDA 510(k) clearance under submission number K191865, sponsored by Dentsply Sirona. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code EBZ and 21 CFR 872.6070, within the Dental review panel as a Class II device.