meddevicedb.com FDA Device Reference

SureSmile Aligner (ASSY500020)

K260722 Class II Traditional
Decision Date
2026-04-15
Sponsor / Applicant
Dentsply Sirona, Inc.

Technical Specification

510(k) Submission ID K260722
Product Code NXC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5470
Decision Date 2026-04-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SureSmile Aligner (ASSY500020) received FDA 510(k) clearance under submission number K260722, sponsored by Dentsply Sirona, 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 2026-04-15.

Classification & Regulation

This clearance is catalogued under FDA product code NXC and 21 CFR 872.5470, within the Dental review panel as a Class II device.