meddevicedb.com FDA Device Reference

Dorsal Appliance

K143591 Class II Traditional
Decision Date
2015-04-15
Sponsor / Applicant
Gergens Orthodontic Lab

Technical Specification

510(k) Submission ID K143591
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2015-04-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Dorsal Appliance received FDA 510(k) clearance under submission number K143591, sponsored by Gergens Orthodontic Lab. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-04-15.

Classification & Regulation

This clearance is catalogued under FDA product code LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.