Transvivo, Inc.
Country not established
- Devices
- 1
What Transvivo, Inc. makes
Transvivo, Inc. manufactures the OMNI-DL System, a device designed for decellularized lung perfusion and processing to facilitate tissue preparation for transplantation or research.
The OMNI-DL System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Omni-Dl System Ref K080650
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transvivo, Inc. have in the registry?
The registry currently lists 1 device for Transvivo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transvivo, Inc.'s devices?
Among its 1 most recently registered device, Transvivo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Transvivo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Transvivo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transvivo, Inc. in the registry?
The most recently registered devices listed for Transvivo, Inc. include OMNI-DL SYSTEM.