GEORGE TIEMANN & CO.
FDA registration: United States Last updated 25 Oct 2026
- Devices
- 1,708
- Registries
- GUDIDFDA
- FDA recalls
- 0
Catalogue
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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.
Information
- FDA registration
- United States
- Address
- 25 PLANT AVE., HAUPPAUGE, NY, 11788
- FDA FEI number
- 2424531