Flexible Stenting Solutions, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Flexible Stenting Solutions, Inc. makes
Flexible Stenting Solutions, Inc. manufactures biliary self-expanding stent systems designed for use in the biliary tree, including variants for drainage and obstruction relief in patients with conditions such as cholangiocarcinoma or benign biliary strictures.
The company’s products are regulated as Class II medical devices under the FDA’s 510(k) pathway and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Flexstent Biliary Self-Expanding Stent System Ref K112522
Regimes: 510(k) Registry: 510(k)Flexstent Biliary Self-Expanding Stent System Ref K120452
Regimes: 510(k) Registry: 510(k)Flexstent Biliary Self-Expanding Stent System Ref K121125
Regimes: 510(k) Registry: 510(k)Flexstent Biliary Self Expanding Stent System Ref K081996
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Flexible Stenting Solutions, Inc. have in the registry?
The registry currently lists 5 devices for Flexible Stenting Solutions, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Flexible Stenting Solutions, Inc.'s devices?
Among its 5 most recently registered devices, Flexible Stenting Solutions, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Flexible Stenting Solutions, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Flexible Stenting Solutions, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Flexible Stenting Solutions, Inc. in the registry?
The most recently registered devices listed for Flexible Stenting Solutions, Inc. include FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM MODEL FLX-DDLLL-BX, FLEXSTENT BILIARY SELF-EXPANDING STENT SYSTEM and FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM.