meddevicedb.com FDA Device Reference

“FLNT Base” and “FLNT Temp”

K253380 Class II Traditional
Decision Date
2026-03-02
Sponsor / Applicant
Liaoning Upcera Co., Ltd.

Technical Specification

510(k) Submission ID K253380
Product Code EBG
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3770
Decision Date 2026-03-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

“FLNT Base” and “FLNT Temp” received FDA 510(k) clearance under submission number K253380, sponsored by Liaoning Upcera 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 2026-03-02.

Classification & Regulation

This clearance is catalogued under FDA product code EBG and 21 CFR 872.3770, within the Dental review panel as a Class II device.