meddevicedb.com FDA Device Reference

NextDent Base

K231388 Class II Abbreviated
Decision Date
2023-10-20
Sponsor / Applicant
Vertex-Dental B.V.

Technical Specification

510(k) Submission ID K231388
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2023-10-20
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NextDent Base received FDA 510(k) clearance under submission number K231388, sponsored by Vertex-Dental B.V.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2023-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code EBI and 21 CFR 872.3760, within the Dental review panel as a Class II device.