Cleared Traditional

K172530 - BEAUTIFIL Flow Plus X (FDA 510(k) Clearance)

Dec 2017
Decision
107d
Days
Class 2
Risk

K172530 is an FDA 510(k) clearance for the BEAUTIFIL Flow Plus X. 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 December 6, 2017, 107 days after receiving the submission on August 21, 2017.

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

Submission Details

510(k) Number K172530 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 21, 2017
Decision Date December 06, 2017
Days to Decision 107 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