Omnichroma Flow

FDA 510(k) K193537 · Tokuyama Dental Corporation

Substantially Equivalent

510(k) numberK193537

Submission

Device name
Omnichroma Flow
Applicant
Tokuyama Dental Corporation
Tokyo, JP
Received
December 20, 2019
Decision date
August 19, 2020
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EBF – Material, Tooth Shade, Resin
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3690
Specialty
Dental

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K262228Transcend Bulk Fill Flowable CompositeEBF · Traditional Ultradent Products, Inc.07/01/2026SE
K261485Tetric plus Fill;Tetric plus FlowEBF · Traditional Ivoclar Vivadent, Inc.07/01/2026SE
K261246SRGC-06EBF · Traditional GC America, Inc.06/18/2026SE
K261093DiafilEBF · Traditional DiaDent Group International06/02/2026SE
K261071DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW…EBF · Traditional DiaDent Group International05/19/2026SE
K260805Dual CoreEBF · Traditional Vericom Co., Ltd.05/11/2026SE
K261357Grandio disc multicolorEBF · Traditional Voco GmbH04/27/2026SE
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More from Hangzhou SHINING3D Dental Technology Co., Ltd.

510(k)DeviceDecision
K203760Tokuyama Universal Bond IIKLE · Traditional 05/25/2021SE
K203598Omnichroma Flow BulkEBF · Traditional 02/03/2021SE
K190940Tokuyama Rebase IIIEBI · Traditional 10/04/2019SE
K180613Estelite Universal FlowEBF · Traditional 07/12/2018SE
K173275OmnichromaEBF · Traditional 02/27/2018SE
K171226Tokuyama Universal BondKLE · Traditional 11/28/2017SE
K170549Tokuyama CuregraceEBI · Traditional 07/05/2017SE
K161353ESTELITE BULK FILL FlowEBF · Traditional 04/03/2017SE
K150727EstecemEMA · Traditional 06/17/2015SE
K112445Sofreliner Tough SEBI · Traditional 10/28/2011SE

Questions and answers

When was Omnichroma Flow cleared by the FDA?

Omnichroma Flow (K193537) received a 510(k) decision of Substantially Equivalent on August 19, 2020, 243 days after the submission was received.

What is the product code of K193537?

The FDA product code is EBF – Material, Tooth Shade, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3690.