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REST EAZY Appliance

K172760 Class II Traditional
Decision Date
2018-03-26
Sponsor / Applicant
Insert Molding Solutions, Inc.

Technical Specification

510(k) Submission ID K172760
Product Code LRK
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 2018-03-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REST EAZY Appliance received FDA 510(k) clearance under submission number K172760, sponsored by Insert Molding Solutions, 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 2018-03-26.

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.