meddevicedb.com FDA Device Reference

Light Cure Adhesive

K241056 Class II Traditional
Decision Date
2024-07-16
Sponsor / Applicant
Sincera Technology (Changchun) Co., Ltd.

Technical Specification

510(k) Submission ID K241056
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2024-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Light Cure Adhesive received FDA 510(k) clearance under submission number K241056, sponsored by Sincera Technology (Changchun) 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 2024-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.