Feilo Sylvania Germany GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Feilo Sylvania Germany GmbH - FDA 510(k) Cleared Devices
Recent clearances: UV Lamps for Sunlamp Products
1
Total
1
Cleared
0
Denied
Feilo Sylvania Germany GmbH has 1 FDA 510(k) cleared medical devices. Based in Erlangen, DE.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Feilo Sylvania Germany GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nats Corp. as regulatory consultant.
FDA 510(k) Regulatory Record - Feilo Sylvania Germany GmbH
1 devices