Duogenic Stemcells Corporation is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Duogenic Stemcells Corporation - FDA 510(k) Cleared Devices
Recent clearances: “MoFi” Cell Culture Basal Medium
1
Total
1
Cleared
0
Denied
Duogenic Stemcells Corporation has 1 FDA 510(k) cleared medical devices. Based in Taichung City, TW.
Latest FDA clearance: Jul 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Duogenic Stemcells Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Duogenic Stemcells Corporation
1 devices