Modela AG is one of 136 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Modela AG - FDA 510(k) Cleared Devices
Recent clearances: Basic, Dominant Flex
1
Total
1
Cleared
0
Denied
Modela AG has 1 FDA 510(k) cleared medical devices. Based in Baar, CH.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Modela AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pathway Regulatory Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Modela AG
1 devices