Cytomedix
Country not established
- Devices
- 1
What Cytomedix makes
Cytomedix manufactures the Autologel Process Centrifuge, a device designed for processing biological materials, including blood components, to prepare autologous gels for wound care or tissue regeneration applications. The system is intended for use in clinical or procedural settings where autologous matrix products are required.
The company’s portfolio is regulated under Class I medical devices in the United States, with relevant products listed via the FDA’s 510(k) pathway. The manufacturer is based in the US.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Cytomedix have in the registry?
The registry currently lists 1 device for Cytomedix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cytomedix's devices?
Among its 1 most recently registered device, Cytomedix has devices listed in FDA 510(k) (1 device).
What risk classes do Cytomedix's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cytomedix's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cytomedix in the registry?
The most recently registered devices listed for Cytomedix include AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129).