Stradis Healthcare is one of 16378 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stradis Healthcare - FDA 510(k) Cleared Devices
Recent clearances: Unger Quad Injector
1
Total
1
Cleared
0
Denied
Stradis Healthcare has 1 FDA 510(k) cleared medical devices. Based in Lawrenceville, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stradis Healthcare Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wood Burditt Group as regulatory consultant.
FDA 510(k) Regulatory Record - Stradis Healthcare
1 devices