Delfin Technologies, Ltd. is one of 47 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Delfin Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MoistureMeterD Compact, LymphScanner, MoisturemeterD
2
Total
2
Cleared
0
Denied
Delfin Technologies, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Kuopio, FI.
Last cleared in 2022. Active since 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Delfin Technologies, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Buchanan Ingersol and Rooney and F Care Systems USA (Dba: Delfin USA, LLC).
FDA 510(k) Regulatory Record - Delfin Technologies, Ltd.
2 devices