meddevicedb.com FDA Device Reference

Overjet Caries Assist-Pediatric

K233738 Class II Traditional
Decision Date
2024-03-04
Sponsor / Applicant
Overjet, Inc.

Technical Specification

510(k) Submission ID K233738
Product Code MYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2070
Decision Date 2024-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Overjet Caries Assist-Pediatric received FDA 510(k) clearance under submission number K233738, sponsored by Overjet, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-03-04.

Classification & Regulation

This clearance is catalogued under FDA product code MYN and 21 CFR 892.2070, within the Radiology review panel as a Class II device.