Vescare, Inc.
Country not established
- Devices
- 1
What Vescare, Inc. makes
Vescare, Inc. manufactures the GRAFTSAVER, a device designed for preserving and protecting tissue grafts during surgical procedures.
The GRAFTSAVER is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Graftsaver Ref K043515
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vescare, Inc. have in the registry?
The registry currently lists 1 device for Vescare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vescare, Inc.'s devices?
Among its 1 most recently registered device, Vescare, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vescare, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vescare, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vescare, Inc. in the registry?
The most recently registered devices listed for Vescare, Inc. include GRAFTSAVER.