Hellige GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Hellige GmbH - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Hellige GmbH has 2 FDA 510(k) cleared medical devices. Based in D7800 Freiburg Im Breisga, DE.
Historical record: 2 cleared submissions from 1995 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hellige GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hellige GmbH
2 devices