Cleared Traditional

K180065 - FUSION Plus Curing Light (FDA 510(k) Clearance)

Apr 2019
Decision
465d
Days
Class 2
Risk

K180065 is an FDA 510(k) clearance for the FUSION Plus Curing Light. This device is classified as a Activator, Ultraviolet, For Polymerization (Class II - Special Controls, product code EBZ).

Submitted by Dentlight, Inc. (Plano, US). The FDA issued a Cleared decision on April 19, 2019, 465 days after receiving the submission on January 9, 2018.

This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.6070.

Submission Details

510(k) Number K180065 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 09, 2018
Decision Date April 19, 2019
Days to Decision 465 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code EBZ - Activator, Ultraviolet, For Polymerization
Device Class Class II - Special Controls
CFR Regulation 21 CFR 872.6070