GEORGE TIEMANN & CO.

FDA registration: United States Last updated 25 Oct 2026

Devices: 1,708
Registries: GUDIDFDA
FDA recalls: 0

Catalogue1,708

Page 6 of 35

Showing 251-300 of 1,708

What GEORGE TIEMANN & CO. makes

GEORGE TIEMANN & CO. makes medical devices such as titanium bone screws.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

FDA registration: United States(from the FDA establishment record (FEI))
Address: 25 PLANT AVE., HAUPPAUGE, NY, 11788
FDA FEI number: 2424531

Catalogue1,708

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What GEORGE TIEMANN & CO. makes

Information