Data / Medical devices / United States / George Taub Products & Fusion Co., Inc.

George Taub Products & Fusion Co., Inc.: FDA-registered device maker in Jersey City, NJ, United States, 8 510(k) clearances

Name: George Taub Products & Fusion Co., Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

George Taub Products & Fusion Co., Inc. is registered with the FDA (registration 2241860) in Jersey City, NJ, United States. It lists 21 device types. The FDA files 8 510(k) clearances under its listings, the newest dated February 26, 2016. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch George Taub Products & Fusion Co., Inc.

FDA registration number: 2241860
Address: 277 New York Ave, Jersey City, NJ, United States, 07307
Owner or operator: GEORGE TAUB PRODUCTS & FUSION CO., INC. (2241860)
Roles: Manufacturer, Repackager or relabeler
First device listed: December 1, 1992
Registered through: 2026
Brand names listed: BALL BURNISHER, BRIGHT SPOT I, BRIGHT SPOT II, BRIGHT SPOT III, BRIGHT SPOT IV, BRIGHT SPOT V, BRIGHT SPOT VI, Denture Base Staining Kit and more

Devices it lists

Device	Product code	Class	Role	Source
Absorber, Saliva, Paper	KHR	1	Repackager or relabeler	accessdata.fda.gov
Agent, Polishing, Abrasive, Oral Cavity	EJR	1	Repackager or relabeler	accessdata.fda.gov
Applicator, Resin	KXR	1	Repackager or relabeler	accessdata.fda.gov
Burnisher, Operative	EKJ	1	Repackager or relabeler	accessdata.fda.gov
Carver, Wax, Dental	EIK	1	Repackager or relabeler	accessdata.fda.gov
Cement, Dental	EMA	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Coating, Filling Material, Resin	EBD	2	Manufacturer	accessdata.fda.gov
Dam, Rubber	EIE	1	Manufacturer	accessdata.fda.gov
Denture Preformed (Partially Prefabricated Denture)	EKO	2	Manufacturer	accessdata.fda.gov
Denture Repair Kit	EBO	2	Manufacturer	accessdata.fda.gov
External Cleaning Solution	PME	2	Manufacturer	accessdata.fda.gov
File, Margin Finishing, Operative	EKA	1	Manufacturer	accessdata.fda.gov
Instruments, Dental Hand	DZN	1	Repackager or relabeler	accessdata.fda.gov
Liner, Cavity, Calcium Hydroxide	EJK	2	Manufacturer	accessdata.fda.gov
Material, Tooth Shade, Resin	EBF	2	Manufacturer	accessdata.fda.gov
Needle, Dental	DZM	1	Repackager or relabeler	accessdata.fda.gov
Paper, Articulation	EFH	1	Manufacturer	accessdata.fda.gov
Remover, Crown	EIS	1	Repackager or relabeler	accessdata.fda.gov
Retractor, All Types	EIG	1	Repackager or relabeler	accessdata.fda.gov
Sealant, Pit And Fissure, And Conditioner	EBC	2	Repackager or relabeler	accessdata.fda.gov
Syringe, Restorative And Impression Material	EID	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
February 26, 2016	K153191	Calcium Bridge	EBF	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
February 18, 2016	K151945	Triumph Resin Dam	EIE	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
December 16, 2015	K152322	Resolve 2.0	PME	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
November 10, 2014	K141503	DENALI 501CEMENT	EMA	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
March 14, 2014	K132393	CERCOM II CEMENT	EMA	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
January 17, 2008	K073101	AURAVENEER CEMENT	EMA	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
June 5, 2007	K071158	AURALAY PIT & FISSURE SEALANT	EBC	Substantially Equivalent	Denali Corporation	accessdata.fda.gov
February 4, 1986	K854588	INSTA-GLAZE	EJR	Substantially Equivalent	George Taub Products & Fusion Co., Inc.	accessdata.fda.gov

Compare with other makers

Updated February 26, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.