Hemoshpere, Inc., A Cryolife Company
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- Devices
- 1
What Hemoshpere, Inc., A Cryolife Company makes
Hemoshpere, Inc., A Cryolife Company produces the HERO GRAFT, which is a Class II medical device.
The HERO GRAFT is listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Hero Graft Ref K124039
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemoshpere, Inc., A Cryolife Company have in the registry?
The registry currently lists 1 device for Hemoshpere, Inc., A Cryolife Company. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemoshpere, Inc., A Cryolife Company's devices?
Among its 1 most recently registered device, Hemoshpere, Inc., A Cryolife Company has devices listed in FDA 510(k) (1 device).
What risk classes do Hemoshpere, Inc., A Cryolife Company's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemoshpere, Inc., A Cryolife Company's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemoshpere, Inc., A Cryolife Company in the registry?
The most recently registered devices listed for Hemoshpere, Inc., A Cryolife Company include HERO GRAFT.