Medtronic Instent, Inc.
Country not established
- Devices
- 1
What Medtronic Instent, Inc. makes
Medtronic Instent, Inc. manufactures the Esophacoil Esophageal Stent System with Slow Release, a device designed for the placement of expandable stents in the esophagus to relieve obstructions or fistulas.
The company’s portfolio is regulated under FDA Class II devices, with the Esophacoil system authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Instent, Inc. have in the registry?
The registry currently lists 1 device for Medtronic Instent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Instent, Inc.'s devices?
Among its 1 most recently registered device, Medtronic Instent, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Instent, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Instent, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Instent, Inc. in the registry?
The most recently registered devices listed for Medtronic Instent, Inc. include MEDTRONIC INSTENT ESOPHACOIL ESOPHAGEAL STENT SYSTEM WITH SLOW RELEASE.