Vpi
Country not established
- Devices
- 2
What Vpi makes
Vpi manufactures devices for urinary tract interventions, including percutaneous retrograde nephrostomy catheters and balloon dilation tools for helical stone extraction. These products are designed for minimally invasive procedures to manage kidney stones and related obstructions.
The company’s portfolio is regulated under FDA’s Class II and Unclassified (U) categories, with devices listed via the 510(k) pathway. These products are intended for use in the United States.
Catalogue
Percutaneous Retrograde Nephrostomy Ref K833762
510(k) 510(k)Balloon Dilation Helical Stone Extract Ref K831875
510(k) 510(k)
Frequently asked questions
How many devices does Vpi have in the registry?
The registry currently lists 2 devices for Vpi. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vpi's devices?
Among its 2 most recently registered devices, Vpi has devices listed in FDA 510(k) (2 devices).
What risk classes do Vpi's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vpi's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vpi in the registry?
The most recently registered devices listed for Vpi include PERCUTANEOUS RETROGRADE NEPHROSTOMY and BALLOON DILATION HELICAL STONE EXTRACT.