A&E Specialty Fabricators
Country not established
- Devices
- 1
What A&E Specialty Fabricators makes
A&E Specialty Fabricators manufactures MRI-compatible shielding materials and components designed to enhance imaging safety and quality, specifically the MRI ULTRAVIEW series. These products are engineered to reduce radiofrequency interference and improve signal clarity in magnetic resonance imaging environments.
The company’s portfolio is regulated under Class II medical devices in the United States, with relevant products authorised via 510(k) clearance through the FDA. The manufacturer operates within the US regulatory framework and is based in the United States.
Catalogue
Mri Ultraview Ref K915260
510(k) 510(k)
Frequently asked questions
How many devices does A&E Specialty Fabricators have in the registry?
The registry currently lists 1 device for A&E Specialty Fabricators. Devices recorded under merged duplicate company entries are counted once.
Which registries list A&E Specialty Fabricators's devices?
Among its 1 most recently registered device, A&E Specialty Fabricators has devices listed in FDA 510(k) (1 device).
What risk classes do A&E Specialty Fabricators's devices fall under?
Among its 1 most recently registered device, the classes recorded for A&E Specialty Fabricators's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A&E Specialty Fabricators in the registry?
The most recently registered devices listed for A&E Specialty Fabricators include MRI ULTRAVIEW.