meddevicedb.com FDA Device Reference

DD Solid Connect® CAD/CAM Abutments (further DD Ti-Base 2CUT series)

K230218 Class II Traditional
Decision Date
2023-04-25
Sponsor / Applicant
Dental Direkt GmbH

Technical Specification

510(k) Submission ID K230218
Product Code NHA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3630
Decision Date 2023-04-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DD Solid Connect® CAD/CAM Abutments (further DD Ti-Base 2CUT series) received FDA 510(k) clearance under submission number K230218, sponsored by Dental Direkt GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2023-04-25.

Classification & Regulation

This clearance is catalogued under FDA product code NHA and 21 CFR 872.3630, within the Dental review panel as a Class II device.