Stemics S.A.S is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Stemics S.A.S - FDA 510(k) Cleared Devices
Recent clearances: KTA Adipose Treatment Kit
1
Total
1
Cleared
0
Denied
Stemics S.A.S has 1 FDA 510(k) cleared medical devices. Based in Besancon, FR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stemics S.A.S Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gloster Biomedical International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Stemics S.A.S
1 devices