Butler Calci-Flor Prophylaxis Paste

FDA 510(k) K102053 · Sunstar Americas, Inc.

Substantially Equivalent

510(k) numberK102053

Submission

Device name
Butler Calci-Flor Prophylaxis Paste
Applicant
Sunstar Americas, Inc.
Lake Bluff, IL, US
Received
July 22, 2010
Decision date
February 3, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EJR – Agent, Polishing, Abrasive, Oral Cavity
Device class
Class I (low risk)
Regulation
21 CFR 872.6030
Specialty
Dental

Other 510(k)s with product code EJR

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K171189AIR-FLOW PLUS Prophylaxis powderEJR · Traditional E.M.S Electro Medical Systems S.A09/11/2017SE
K131760Whip Mix Preppies PlusEJR · Traditional Whip-Mix Corp.03/26/2014SE
K121698Nupro Sensodyne Prophylaxis Paste with NovaminEJR · Traditional Dentsply International, Inc.08/06/2012SE
K103114Osspray Sylc CREJR · Traditional Osspray, Ltd.03/14/2011SE
K101104Remin ProEJR · Traditional Voco GmbH10/21/2010SE
K100539Preventech Prophylaxis Paste with FluorideEJR · Traditional Preventive Technologies, Inc.06/17/2010SE
K070854GC Mi Paste PlusEJR · Special GC America, Inc.04/12/2007SE
K062502Osspray Cleaning CompoundEJR · Traditional Ospray, Ltd.12/15/2006SE
K062166Enamel ProEJR · Traditional Premier Dental Products Co.11/21/2006SE
K042048Gelato Prophylaxis PasteEJR · Traditional Deepak Products, Inc.10/26/2004SE

More from Deepak Products, Inc.

510(k)DeviceDecision
K181134G•U•M HYDRAL Dry Mouth Oral Gel, G•U•M HYDRAL Dry Mouth Oral Rinse, G•U•M HYDRAL Dry…LFD · Traditional 07/13/2018SE
K132325Guidor Bioresorbable Matrix BarrierNPK · Abbreviated 10/29/2013SE

Questions and answers

When was Butler Calci-Flor Prophylaxis Paste cleared by the FDA?

Butler Calci-Flor Prophylaxis Paste (K102053) received a 510(k) decision of Substantially Equivalent on February 3, 2011, 196 days after the submission was received.

What is the product code of K102053?

The FDA product code is EJR – Agent, Polishing, Abrasive, Oral Cavity, a Class I (low risk) device regulated under 21 CFR 872.6030.