Xenolith Medical
IsraelFDA applicant, unverified
- Devices
- 2
What Xenolith Medical makes
Xenolith Medical produces the XENX Stone Management Device and the XENX, which are designed for percutaneous treatment of urinary stones, including fragmentation and retrieval procedures.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Xenx Stone Management Device Ref K123438
Regimes: 510(k) Registry: 510(k)Xenx Ref K113692
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Xenolith Medical have in the registry?
The registry currently lists 2 devices for Xenolith Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xenolith Medical's devices?
Among its 2 most recently registered devices, Xenolith Medical has devices listed in FDA 510(k) (2 devices).
What risk classes do Xenolith Medical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Xenolith Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xenolith Medical in the registry?
The most recently registered devices listed for Xenolith Medical include XENX STONE MANAGEMENT DEVICE and XENX.