Exogenesis Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Exogenesis Corporation - FDA 510(k) Cleared Devices
Recent clearances: Exogenesis Hernia Mesh
1
Total
1
Cleared
0
Denied
Exogenesis Corporation has 1 FDA 510(k) cleared medical devices. Based in Billerica, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Exogenesis Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Exogenesis Corporation
1 devices