Microvas Systems, Inc.
Country not established
- Devices
- 1
What Microvas Systems, Inc. makes
Microvas Systems, Inc. manufactures the MSI MAGNA-STYM, a surgical adhesive designed for tissue approximation and wound closure in medical procedures.
The company’s portfolio is regulated under FDA’s Class II device classification, with the MSI MAGNA-STYM authorised via the 510(k) pathway. The product is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Msi Magna-Stym Ref K972055
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microvas Systems, Inc. have in the registry?
The registry currently lists 1 device for Microvas Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microvas Systems, Inc.'s devices?
Among its 1 most recently registered device, Microvas Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Microvas Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Microvas Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microvas Systems, Inc. in the registry?
The most recently registered devices listed for Microvas Systems, Inc. include MSI MAGNA-STYM.