Uniphy Elektromedizin GmbH & Co. KG is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Uniphy Elektromedizin GmbH & Co. KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Uniphy Elektromedizin GmbH & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Bilzen, BE.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Uniphy Elektromedizin GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Uniphy Elektromedizin GmbH & Co. KG
1 devices