Schneider U.S. Stent Div.
Country not established
- Devices
- 3
What Schneider U.S. Stent Div. makes
Schneider U.S. Stent Div. manufactures self-expanding metallic stents for biliary and esophageal applications, including biliary endoprostheses, esophageal prostheses, and trans-biliary stents with delivery systems.
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
Wallstent Biliary Endoprotheses Ref K923993
Regimes: 510(k) Registry: 510(k)Wallstent Esophageal Prothesis Ref K923119
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schneider U.S. Stent Div. have in the registry?
The registry currently lists 3 devices for Schneider U.S. Stent Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schneider U.S. Stent Div.'s devices?
Among its 3 most recently registered devices, Schneider U.S. Stent Div. has devices listed in FDA 510(k) (3 devices).
What risk classes do Schneider U.S. Stent Div.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Schneider U.S. Stent Div.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schneider U.S. Stent Div. in the registry?
The most recently registered devices listed for Schneider U.S. Stent Div. include WALLSTENT BILIARY ENDOPROTHESES, WALLSTENT ESOPHAGEAL PROTHESIS and WALLSTENT(R) TRANS BILIARY ENDO W/UNISTEP DELIV SY.