Instent, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Instent, Inc. makes
Instent, Inc. manufactures self-expanding stent systems and endoprostheses for biliary and esophageal applications, including the EndoCoil Biliary Endoprosthesis, Esophacoil Esophageal Prosthesis, and EndoCoil-T Transhepatic Biliary Endoprosthesis.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Instent Endocoil Biliary Endoprosthesis Ref K924387
Regimes: 510(k) Registry: 510(k)Instent Esophacoil Esophageal Prosthesis Ref K941487
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Instent Esophacoil Self-Expanding Stent System Ref K955041
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Instent, Inc. have in the registry?
The registry currently lists 4 devices for Instent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Instent, Inc.'s devices?
Among its 4 most recently registered devices, Instent, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Instent, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Instent, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Instent, Inc. in the registry?
The most recently registered devices listed for Instent, Inc. include INSTENT ENDOCOIL BILIARY ENDOPROSTHESIS, INSTENT ESOPHACOIL ESOPHAGEAL PROSTHESIS, INSTENT ENDOCOIL-T(TM) TRANSHEPATIC BILIARY ENDOPROSTHESIS and INSTENT ESOPHACOIL SELF-EXPANDING STENT SYSTEM.