meddevicedb.com FDA Device Reference

I-View Gold and Imagen Gold Dental Sensors

K200625 Class II Traditional
Decision Date
2020-04-15
Sponsor / Applicant
Trident S.R.L

Technical Specification

510(k) Submission ID K200625
Product Code MUH
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2020-04-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

I-View Gold and Imagen Gold Dental Sensors received FDA 510(k) clearance under submission number K200625, sponsored by Trident S.R.L. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2020-04-15.

Classification & Regulation

This clearance is catalogued under FDA product code MUH and 21 CFR 872.1800, within the Dental review panel as a Class II device.