Stage 2 Innovations is one of 18553 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stage 2 Innovations - FDA 510(k) Cleared Devices
Recent clearances: Renew NCP-5 External Counterpulsation System
1
Total
1
Cleared
0
Denied
Stage 2 Innovations has 1 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Stage 2 Innovations Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Stage 2 Innovations
1 devices