Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2241860

FEI Number

2241860

Entity Name

GEORGE TAUB PRODUCTS & FUSION CO., INC.

City/State/Country

JERSEY CITY, NJ, US

Establishment Address

277 New York Ave, JERSEY CITY, NJ 07307, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

GEORGE TAUB PRODUCTS & FUSION CO., INC. (Owner Number: 2241860)

Owner / Operator Contact Address

277 NEW YORK AVE., --, Jersey City, NJ 07307, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BALL BURNISHER TENDER SPOT BRIGHT SPOT V BRIGHT SPOT VI BRIGHT SPOT IV BRIGHT SPOT III BRIGHT SPOT II BRIGHT SPOT I Mouth Gag - Molt Trident - Mouth Props Tru-Paque HYDROXYLINE TC HYDROXYLINE Inlay/Onlay Styx Veneer Styx SAL-DRI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PME	External Cleaning Solution	Dental	Class 2	872.3260	2015-12-29
EKJ	Burnisher, Operative	Dental	Class 1	872.4565	1992-12-01
EBF	Material, Tooth Shade, Resin	Dental	Class 2	872.3690	2016-03-01
EFH	Paper, Articulation	Dental	Class 1	872.6140	2006-01-10
EMA	Cement, Dental	Dental	Class 2	872.3275	2013-11-21
EMA	Cement, Dental	Dental	Class 2	872.3275	2014-11-20
EIG	Retractor, All Types	Dental	Class 1	872.4565	2020-05-22
EBF	Material, Tooth Shade, Resin	Dental	Class 2	872.3690	2007-12-21
EJK	Liner, Cavity, Calcium Hydroxide	Dental	Class 2	872.3250	2007-12-21
EJR	Agent, Polishing, Abrasive, Oral Cavity	Dental	Class 1	872.6030	2015-05-14
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	1992-12-01
EMA	Cement, Dental	Dental	Class 2	872.3275	2014-11-20
EIE	Dam, Rubber	Dental	Class 1	872.6300	2016-02-20
KHR	Absorber, Saliva, Paper	Dental	Class 1	872.6050	1992-12-01

Official Correspondent

LAWRENCE TAUB

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GEORGE TAUB PRODUCTS & FUSION CO., INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K952662	Jeneric/Pentron, Inc.	COMP=FLOW	1995-08-28
K171147	Bisco, Inc.	REVEAL Bulk	2017-08-04
K770922	Espe GmbH (Us)	DENTAL RESTORATIVE IN CAPSULES	1977-06-01
K153476	Kuraray Noritake Dental, Inc.	KATANA AVENCIA Block	2016-08-23
K972485	Arent, Fox, Kintner, Plotkin & Kahn	CIMPAT N	1997-09-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0028-2020	Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany	2	Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all classes - Filling small class I cavities and extended fissure sealing - Filling class II - V cavities including V-shaped defects and cervical caries - Blocking out undercuts - Lining or coating cavities - Repairing fillings and veneers - Luting translucent prosthetic pieces (e.g., full ceramic crowns, etc.).

Similar Registrations

Registration Number	Establishment Name	Location
3002807420	KURARAY NORITAKE DENTAL NIIGATA PLANT	TAINAI Niigata, JP
3006367836	DENALI R & D CORPORATION	Hanover, MA, US
1420052	BISCO, INC.	Schaumburg, IL, US
3005176727	IMICRYL DIS MALZEMELERI SANAYI VE TICARET A.S.	Konya, TR
3012996495	VIARDEN LAB LLC	Mission, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2241860. Last updated year: 2026. Please use registration number 2241860 when referencing this establishment in official correspondence.