Sonifloss

FDA 510(k) K935148 · American Dentronics, Inc.

Substantially Equivalent

510(k) numberK935148

Submission

Device name
Sonifloss
Applicant
American Dentronics, Inc.
Las Vegas, NV, US
Received
October 28, 1993
Decision date
January 31, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JEQ – Toothbrush, Powered
Device class
Class I (low risk)
Regulation
21 CFR 872.6865
Specialty
Dental

Other 510(k)s with product code JEQ

510(k)DeviceApplicantDecision
K200881Oral-B iO Test Drive Power Brush Trial Program KitJEQ · Traditional The Procter & Gamble Company08/27/2020SE
K141018Oral-B Test Drive Power Brush Trial Program Kit, Oral-B Test Drive Power Toothbrush Kit…JEQ · Traditional Procter & Gamble Co.09/15/2014SE
K061351Oral-B Sonic CompleteJEQ · Traditional Braun GmbH06/05/2006SE
K061199Oral B Professionalcare Series, Oral B Advancepower SeriesJEQ · Traditional Braun GmbH05/31/2006SE
K040416Sonicare Advance Toothbrush, Model 4900JEQ · Traditional Philips Oral Healthcare, Inc.07/02/2004SE
K022900Butler Gum Vari-Clean Power ToothbrushesJEQ · Traditional John O. Butler Co.11/14/2002SE
K012914Sonicwave Sonic Plaque RemoverJEQ · Traditional Homedics, Inc.10/01/2001SE
K970381Powered ToothbrushJEQ · Traditional Emjoi Action USA, Ltd.04/18/1997SE
K943942Trav-Ler KitJEQ · Traditional John O. Butler Co.03/08/1995SESK
K945248Hukuba Hyg Electric Ionic ToothbrushJEQ · Traditional Hukuba Dental Corp.01/26/1995SE

More from Hukuba Dental Corp.

510(k)DeviceDecision
K980075CybersonicLCN · Traditional 03/04/1998SE
K935150SoniplakJEQ · Traditional 05/18/1994SE
K935149SonibrushJEQ · Traditional 01/31/1994SE

Questions and answers

When was Sonifloss cleared by the FDA?

Sonifloss (K935148) received a 510(k) decision of Substantially Equivalent on January 31, 1994, 95 days after the submission was received.

What is the product code of K935148?

The FDA product code is JEQ – Toothbrush, Powered, a Class I (low risk) device regulated under 21 CFR 872.6865.