FDA applicant

George Tiemann & Co.

Plainview, NY1 decision1985–19850 recalls

FDA records 1 decision for George Tiemann & Co. (Plainview, NY) in 1985: 1 510(k) clearance. All are in product code HWC (Screw, Fixation, Bone). 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, orthopedic panel, where it files most

How often FDA has decided George Tiemann & Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for George Tiemann & Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — George Tiemann & Co. 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 Taub Products & Fusion Co., Inc. 2 George Courey, Inc. 2 George H. Frisch 2 George Glove Company, Inc. 1 George Percy Mcgown 1 George Loo, MD 1 George J. Kamilar 1 George C. Kuhn 1 George W. Cottrell 1

George Tiemann & Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “George”