Brotherston/Pxi
Country not established
- Devices
- 2
What Brotherston/Pxi makes
Brotherston/Pxi manufactures pneumatic compression devices, including the PXI Pneumatic Compression Paddle for therapeutic compression therapy and the PXI URCD, a lower extremity compression system designed for venous insufficiency management.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. These products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations.
Catalogue
Pxi Pneumatic Compression Paddle Ref K913436
510(k) 510(k)Pxi Urcd Ref K913435
510(k) 510(k)
Frequently asked questions
How many devices does Brotherston/Pxi have in the registry?
The registry currently lists 2 devices for Brotherston/Pxi. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brotherston/Pxi's devices?
Among its 2 most recently registered devices, Brotherston/Pxi has devices listed in FDA 510(k) (2 devices).
What risk classes do Brotherston/Pxi's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Brotherston/Pxi's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brotherston/Pxi in the registry?
The most recently registered devices listed for Brotherston/Pxi include PXI PNEUMATIC COMPRESSION PADDLE and PXI URCD.