Beam Brush/Beam App

FDA 510(k) K121165 · Beam Technologies, LLC

Substantially Equivalent

510(k) numberK121165

Submission

Device name
Beam Brush/Beam App
Applicant
Beam Technologies, LLC
Louisville, KY, US
Received
April 17, 2012
Decision date
June 21, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EFW – Toothbrush, Manual
Device class
Class I (low risk)
Regulation
21 CFR 872.6855
Specialty
Dental

Other 510(k)s with product code EFW

510(k)DeviceApplicantDecision
K130186Dentek Easy Brush with FluorideEFW · Traditional Den Tek Oral Care, Inc.07/15/2013SE
K102871Silver Care Anitbacterial ToothbrushEFW · Traditional Piave Spazzolificio S.P.A.10/03/2011SE
K073224Oral-B Sub-Brand Manual ToothbrushEFW · Traditional Procter & Gamble02/06/2008SE
K021383Zeodyne Toothbrush with Agion AntimicrobialEFW · Traditional Agion Technologies, LLC07/17/2002SE
K020776Medoral Hygienic Toothbrush with Dentosan FilamentsEFW · Traditional Coronet Group North America, LLC06/03/2002SE
K000290Lazersmile, LazerwhiteEFW · Traditional Biolase Technology, Inc.04/14/2000SE
K994144Toothbrush WashEFW · Traditional Cal Huech, Inc.03/02/2000SE
K992435Bacti-Stop Toothbrush Cleaner and SanitizerEFW · Traditional Azo Enterprises10/15/1999SE
K980995Plaq-Ataq-IEFW · Traditional Ethicare08/20/1998SE
K974761Butler Antibacterial Interdental ToothbrushEFW · Traditional John O. Butler Co.06/16/1998SE

Questions and answers

When was Beam Brush/Beam App cleared by the FDA?

Beam Brush/Beam App (K121165) received a 510(k) decision of Substantially Equivalent on June 21, 2012, 65 days after the submission was received.

What is the product code of K121165?

The FDA product code is EFW – Toothbrush, Manual, a Class I (low risk) device regulated under 21 CFR 872.6855.