Stemcor Systems, Inc.
Country not established
- Devices
- 1
What Stemcor Systems, Inc. makes
Stemcor Systems, Inc. manufactures the MARROWMINER, a device designed for the processing and preparation of bone marrow aspirate for regenerative medicine applications.
The MARROWMINER is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Marrowminer Ref K071732
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stemcor Systems, Inc. have in the registry?
The registry currently lists 1 device for Stemcor Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stemcor Systems, Inc.'s devices?
Among its 1 most recently registered device, Stemcor Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Stemcor Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stemcor Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Stemcor Systems, Inc. in the registry?
The most recently registered devices listed for Stemcor Systems, Inc. include MARROWMINER.