Cleared Traditional

RODIN Titan 3D Resin

Jun 2024
Decision
99d
Days
Class 2
Risk

About This 510(k) Submission

K240688 is an FDA 510(k) clearance for the RODIN Titan 3D Resin, a Resin, Denture, Relining, Repairing, Rebasing (Class II — Special Controls, product code EBI), submitted by Belport Company, Inc., Gingi-Pak (Brea, US). The FDA issued a Cleared decision on June 20, 2024, 99 days after receiving the submission on March 13, 2024. This device falls under the Dental review panel. Regulated under 21 CFR 872.3760.

Submission Details

510(k) Number K240688 FDA.gov
FDA Decision Cleared SESE
Date Received March 13, 2024
Decision Date June 20, 2024
Days to Decision 99 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code EBI — Resin, Denture, Relining, Repairing, Rebasing
Device Class Class II — Special Controls
CFR Regulation 21 CFR 872.3760

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