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GEORGE TIEMANN & CO.

FDA registration: United States Last updated 25 Oct 2026

Devices
1,708
Registries
GUDIDFDA
FDA recalls
0

Catalogue1,708

Page 29 of 35

Showing 1,401-1,450 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