Msi, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Msi, Inc. makes
Msi, Inc. manufactures the MSI Procedure Kit, a specialized assembly of tools and components for medical procedures, and the Introstat Lead Introducer, a device designed for inserting leads into the body for diagnostic or therapeutic purposes.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance pathway. These devices are registered in the United States.
Catalogue
Msi Procedure Kit Ref K944226
Regimes: 510(k) Registry: 510(k)DURAMESH Mesh Suture Ref K211178
Regimes: 510(k) Registry: 510(k)Introstat Lead Introducer Ref K960200
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Msi, Inc. have in the registry?
The registry currently lists 3 devices for Msi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Msi, Inc.'s devices?
Among its 3 most recently registered devices, Msi, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Msi, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Msi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Msi, Inc. in the registry?
The most recently registered devices listed for Msi, Inc. include MSI PROCEDURE KIT, DURAMESH Mesh Suture and INTROSTAT LEAD INTRODUCER.