meddevicedb.com FDA Device Reference

LumiCare Caries Diagnostic Rinse

K200601 Class II Traditional
Decision Date
2021-03-29
Sponsor / Applicant
GreenMark Biomedical, Inc.

Technical Specification

510(k) Submission ID K200601
Product Code LFC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1740
Decision Date 2021-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LumiCare Caries Diagnostic Rinse received FDA 510(k) clearance under submission number K200601, sponsored by GreenMark Biomedical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code LFC and 21 CFR 872.1740, within the Dental review panel as a Class II device.