Riva Silver

FDA 510(k) K042452 · Southern Dental Industries, Inc.

Substantially Equivalent

510(k) numberK042452

Submission

Device name
Riva Silver
Applicant
Southern Dental Industries, Inc.
Bensenville, IL, US
Received
September 10, 2004
Decision date
December 7, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EMA – Cement, Dental
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3275
Specialty
Dental

Other 510(k)s with product code EMA

510(k)DeviceApplicantDecision
K254201Any-CemEMA · Traditional Mediclus Co., Ltd.08/13/2026SE
K261937PacTemp Automix NEEMA · Traditional The Belport Company Inc., DBA Gingi-Pak08/07/2026SE
K261166Dia-CemEMA · Traditional DiaDent Group International07/09/2026SE
K254109G-Cem UniversalEMA · Traditional GC America, Inc.05/18/2026SE
K253337REGEN Bioactive CementEMA · Traditional Inter-Med, Inc.04/15/2026SE
K252606Bifix Veneer LC, Bifix Veneer Try-InEMA · Traditional Voco GmbH03/20/2026SE
K254063iCEM Universal PlusEMA · Abbreviated Kulzer, LLC12/19/2025SE
K252785TopCEM Vigor SA Self-Adhesive Resin CementEMA · Traditional Rizhao Huge Biomaterials Company, Ltd.12/12/2025SE
K252808GlasIonomer FX-LCEMA · Traditional Shofu Dental Corporation12/09/2025SE
K252165Zirconomer PEMA · Traditional Shofu Dental Corporation10/28/2025SE

More from Shofu Dental Corporation

510(k)DeviceDecision
K062065Riva Luting PlusEMA · Traditional 11/15/2006SE
K062064Riva Bond LCEMA · Traditional 11/09/2006SE
K051008SetEMA · Traditional 06/15/2005SE
K050871Riva ProtectEBC · Traditional 06/10/2005SE
K050870Riva Light CureEMA · Traditional 06/03/2005SE
K050331Adhesive 1KLE · Traditional 03/24/2005SE
K040393Riva LutingEMA · Traditional 04/30/2004SE
K032152Benco AdmixEJJ · Traditional 08/06/2003SE
K031658Benco SphericalEJJ · Traditional 07/29/2003SE
K030568RadiiEBZ · Traditional 04/24/2003SE

Questions and answers

When was Riva Silver cleared by the FDA?

Riva Silver (K042452) received a 510(k) decision of Substantially Equivalent on December 7, 2004, 88 days after the submission was received.

What is the product code of K042452?

The FDA product code is EMA – Cement, Dental, a Class II (moderate risk) device regulated under 21 CFR 872.3275.