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ClearClub Impression Material

K261888 Class II Traditional
Decision Date
2026-09-16
Sponsor / Applicant
ClearClub

Technical Specification

510(k) Submission ID K261888
Product Code SHI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2026-09-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ClearClub Impression Material received FDA 510(k) clearance under submission number K261888, sponsored by ClearClub. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2026-09-16.

Classification & Regulation

This clearance is catalogued under FDA product code SHI and 21 CFR 872.3660, within the Dental review panel as a Class II device.