meddevicedb.com FDA Device Reference

Better Diagnostics Dental Assist (BDDA) Version 1.0

K260851 Class II Traditional
Decision Date
2026-07-15
Sponsor / Applicant
Better Diagnostics AI Corp.

Technical Specification

510(k) Submission ID K260851
Product Code MYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2070
Decision Date 2026-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Better Diagnostics Dental Assist (BDDA) Version 1.0 received FDA 510(k) clearance under submission number K260851, sponsored by Better Diagnostics AI Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-07-15.

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.