meddevicedb.com FDA Device Reference

VSP System (Titanium Palatal Splint)

K261826 Class II Traditional
Decision Date
2026-06-03
Sponsor / Applicant
3D Systems, Inc.

Technical Specification

510(k) Submission ID K261826
Product Code DZJ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4120
Decision Date 2026-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VSP System (Titanium Palatal Splint) received FDA 510(k) clearance under submission number K261826, sponsored by 3D Systems, 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 2026-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code DZJ and 21 CFR 872.4120, within the Dental review panel as a Class II device.