Medron, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medron, LLC - FDA 510(k) Cleared Devices
Recent clearances: MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE Dilator
1
Total
1
Cleared
0
Denied
Medron, LLC has 1 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medron, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medron, LLC
1 devices