Iconlab, Inc. is one of 21835 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iconlab, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Reperen Surgical Mesh
1
Total
1
Cleared
0
Denied
Iconlab, Inc. has 1 FDA 510(k) cleared medical devices. Based in Aliso Viejo, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Iconlab, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Extomed, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Iconlab, Inc.
1 devices