FDA applicant

George Taub Products & Fusion Co., Inc.

Mchenry, IL2 decisions1984–19860 recalls

FDA records 2 decisions for George Taub Products & Fusion Co., Inc. (Mchenry, IL) from 1984 to 1986: 2 510(k) clearances. Most are in product codes EJK (Liner, Cavity, Calcium Hydroxide) and EJR (Agent, Polishing, Abrasive, Oral Cavity). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided George Taub Products & Fusion Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for George Taub Products & Fusion Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — George Taub Products & Fusion Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “George”

FDA records each applicant name separately; these may or may not be the same firm.

George King Bio-Medical, Inc. 5 George M. Wilson, Dds 3 George Courey, Inc. 2 George H. Frisch 2 George Glove Company, Inc. 1 George Percy Mcgown 1 George Tiemann & Co. 1 George Loo, MD 1 George J. Kamilar 1 George C. Kuhn 1 George W. Cottrell 1

George Taub Products & Fusion Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “George”