Michael Todd, LP is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Michael Todd, LP - FDA 510(k) Cleared Devices
Recent clearances: Clear Bi-Light
1
Total
1
Cleared
0
Denied
Michael Todd, LP has 1 FDA 510(k) cleared medical devices. Based in Port St Lucie, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Michael Todd, LP Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Michael Todd, LP
1 devices