Tubulicid Blue Label

FDA 510(k) K864050 · Dental Dimensions Supply Co.

Substantially Equivalent

510(k) numberK864050

Submission

Device name
Tubulicid Blue Label
Applicant
Dental Dimensions Supply Co.
Wantagh, NY, US
Received
October 16, 1986
Decision date
December 5, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

510(k)DeviceApplicantDecision
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

More from Jasberry Healthcare Private Limited

510(k)DeviceDecision
K864051Tubulicid Red LabelLBH · Traditional 12/10/1986SE
K864053Tubulitec LinerEJK · Traditional 12/05/1986SE
K864052Tubulitec PrimerLBH · Traditional 12/05/1986SE

Questions and answers

When was Tubulicid Blue Label cleared by the FDA?

Tubulicid Blue Label (K864050) received a 510(k) decision of Substantially Equivalent on December 5, 1986, 50 days after the submission was received.

What is the product code of K864050?

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