Brightwater Medical
Country not established
- Devices
- 18
What Brightwater Medical makes
Brightwater Medical manufactures the ConvertX Nephroureteral Stent System for urinary drainage and the ConvertX Biliary Stent System for bile duct management, both designed for minimally invasive placement in the body.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 18 devicesFrequently asked questions
How many devices does Brightwater Medical have in the registry?
The registry currently lists 18 devices for Brightwater Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brightwater Medical's devices?
Among its 18 most recently registered devices, Brightwater Medical has devices listed in FDA 510(k) (2 devices) and FDA GUDID (16 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Brightwater Medical's devices fall under?
Among its 18 most recently registered devices, the classes recorded for Brightwater Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brightwater Medical in the registry?
The most recently registered devices listed for Brightwater Medical include ConvertX™ Nephroureteral Stent System 8.3F - 10.3F Taper x 24cm, ConvertX™ Nephroureteral Stent System 8.3F - 10.3F Taper x 12cm, ConvertX™ Nephroureteral Stent System 10.3F x 28cm and ConvertX™ Nephroureteral Stent System 10.3F x 14cm.