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George Taub Products & Fusion Co., Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2241860

Devices
2
Registrations
FDA
FDA recalls
0

What George Taub Products & Fusion Co., Inc. makes

George Taub Products & Fusion Co., Inc. manufactures Hydroxyline, a dental material used for bonding and sealing tooth surfaces, and Insta-Glaze, a ceramic coating applied to dental prosthetics for aesthetic and protective finishing.

The company’s portfolio includes Class I and Class II devices, all of which are listed via the FDA’s 510(k) pathway. These products are regulated under U.S. medical device laws and are based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Hydroxyline Ref K833640

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Insta-Glaze Ref K854588

    Active Regimes: 510(k) Registry: 510(k) Class:I

Company details

FDA FEI number
2241860
Address
277 New York Ave, JERSEY CITY, NJ, 07307

Frequently asked questions

How many devices does GEORGE TAUB PRODUCTS & FUSION CO., INC. have in the registry?

The registry currently lists 2 devices for GEORGE TAUB PRODUCTS & FUSION CO., INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list GEORGE TAUB PRODUCTS & FUSION CO., INC.'s devices?

Among its 2 most recently registered devices, GEORGE TAUB PRODUCTS & FUSION CO., INC. has devices listed in FDA 510(k) (2 devices).

What risk classes do GEORGE TAUB PRODUCTS & FUSION CO., INC.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for GEORGE TAUB PRODUCTS & FUSION CO., INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from GEORGE TAUB PRODUCTS & FUSION CO., INC. in the registry?

The most recently registered devices listed for GEORGE TAUB PRODUCTS & FUSION CO., INC. include HYDROXYLINE and INSTA-GLAZE.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.