meddevicedb.com FDA Device Reference

Orthodontic Acrylic 2

K163482 Class II Traditional
Decision Date
2017-05-31
Sponsor / Applicant
Lang Dental Manufacturing Co., Inc.

Technical Specification

510(k) Submission ID K163482
Product Code EBI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3760
Decision Date 2017-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Orthodontic Acrylic 2 received FDA 510(k) clearance under submission number K163482, sponsored by Lang Dental Manufacturing Co., 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 2017-05-31.

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.