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.
Frequently asked questions
What type of products does GEORGE TIEMANN & CO. manufacture?
GEORGE TIEMANN & CO. makes medical devices, such as titanium bone screws, which are classified as Class II devices.
Where is GEORGE TIEMANN & CO. based?
The company is based in the US, where it produces medical devices like titanium bone screws.
Which regulatory registries list GEORGE TIEMANN & CO.'s devices?
The company's devices are listed in the FDA 510(k) registry, indicating they have undergone regulatory review.
How are GEORGE TIEMANN & CO.'s devices classified?
The company's devices, including titanium bone screws, are classified as Class II devices, which undergo a specific level of regulatory scrutiny.
Information
- FDA registration
- United States
- Address
- 25 PLANT AVE., HAUPPAUGE, NY, 11788
- FDA FEI number
- 2424531