GEORGE TIEMANN & CO.

FDA registration: United States Last updated 25 Oct 2026

Devices: 1,708
Registries: GUDIDFDA 510(k)FDA
FDA recalls: 0

Catalogue1,708

Page 35 of 35

N/A B5821607150 Ref B5821607150

Class I FDA UDI Active
N/A 083501 Ref 083501

Class I FDA UDI Active
N/A 105330 Ref 105330

Class I FDA UDI Active
N/A 80420 Ref 80420

Class I FDA UDI Active
N/A 1103036 Ref 1103036

Class I FDA UDI Active
N/A 1057575 Ref 1057575

Class I FDA UDI Active
N/A 015551 Ref 015551

Class I FDA UDI Active
Titaniuim Bone Screw Ref K853869

Class II FDA 510(k) Active

Showing 1,701-1,708 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