Laurus Medical Group is one of 13016 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laurus Medical Group - FDA 510(k) Cleared Devices
Recent clearances: SUTURE APPLICATOR
1
Total
1
Cleared
0
Denied
Laurus Medical Group has 1 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Laurus Medical Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laurus Medical Group
1 devices