PCXX Varnish

FDA 510(k) K113146 · Ross Healthcare, Inc.

Substantially Equivalent

510(k) numberK113146

Submission

Device name
PCXX Varnish
Applicant
Ross Healthcare, Inc.
Blaine, WA, US
Received
October 24, 2011
Decision date
January 23, 2012
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LBH – Varnish, Cavity
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3260
Specialty
Dental

Other 510(k)s with product code LBH

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K262243Profisil FreeLBH · Traditional Kettenbach GmbH & Co. KG09/03/2026SE
K253052Fluoride Varnish (Type A,Type C)LBH · Traditional Nagy Oral Technology Qinhuangdao Co., Ltd.06/11/2026SE
K252073VOCO Profluorid Varnish + BioMinLBH · Traditional Voco GmbH05/01/2026SE
K261404UltraEZLBH · Special Ultradent Products, Inc.04/30/2026SE
K260830APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)LBH · Traditional Sangi Co., Ltd.03/18/2026SE
K250714FluoroDose VarnishLBH · Traditional Centrix, Inc.11/21/2025SE
K243777Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3%…LBH · Traditional Theodent, LLC05/27/2025SE
K241489ReminGelLBH · Traditional Inter-Med, Inc.01/08/2025SE
K241568CrystLCare™ PRO Biorestorative, Fluoride-PlusLBH · Traditional GreenMark Biomedical, Inc.01/02/2025SE
K242913Jasmate® ToothpasteLBH · Traditional Jasberry Healthcare Private Limited11/22/2024SE

Questions and answers

When was PCXX Varnish cleared by the FDA?

PCXX Varnish (K113146) received a 510(k) decision of Substantially Equivalent on January 23, 2012, 91 days after the submission was received.

What is the product code of K113146?

The FDA product code is LBH – Varnish, Cavity, a Class II (moderate risk) device regulated under 21 CFR 872.3260.