Lokki is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Lokki - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Lokki has 2 FDA 510(k) cleared medical devices. Based in Vienne, FR.
Historical record: 2 cleared submissions from 1995 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lokki Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lokki
2 devices