meddevicedb.com FDA Device Reference

FREEPRINT crown

K222877 Class II Traditional
Decision Date
2022-09-23
Sponsor / Applicant
Detax GmbH

Technical Specification

510(k) Submission ID K222877
Product Code EBF
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3690
Decision Date 2022-09-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FREEPRINT crown received FDA 510(k) clearance under submission number K222877, sponsored by Detax 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 2022-09-23.

Classification & Regulation

This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.