Stemics S.A.S.
FranceFDA applicant, unverified
- Devices
- 1
What Stemics S.A.S. makes
Stemics S.A.S makes the KTA Adipose Treatment Kit, a device used for the processing and handling of adipose tissue.
The KTA Adipose Treatment Kit is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
KTA Adipose Treatment Kit Ref K190386
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stemics S.A.S have in the registry?
The registry currently lists 1 device for Stemics S.A.S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stemics S.A.S's devices?
Among its 1 most recently registered device, Stemics S.A.S has devices listed in FDA 510(k) (1 device).
What risk classes do Stemics S.A.S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stemics S.A.S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stemics S.A.S in the registry?
The most recently registered devices listed for Stemics S.A.S include KTA Adipose Treatment Kit.