Cleared Traditional

K251578 - BEAUTIFIL II (FDA 510(k) Clearance)

May 2025
Decision
5d
Days
Class 2
Risk

K251578 is an FDA 510(k) clearance for the BEAUTIFIL II. This device is classified as a Material, Tooth Shade, Resin (Class II - Special Controls, product code EBF).

Submitted by Shofu Dental Corporation (San Marcos, US). The FDA issued a Cleared decision on May 27, 2025, 5 days after receiving the submission on May 22, 2025.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.

Submission Details

510(k) Number K251578 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 22, 2025
Decision Date May 27, 2025
Days to Decision 5 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement

Device Classification

Product Code EBF — Material, Tooth Shade, Resin
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.3690