Chromogenex Plc is one of 520 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Chromogenex Plc - FDA 510(k) Cleared Devices
Recent clearances: CHROMOLITE SYSTEM
1
Total
1
Cleared
0
Denied
Chromogenex Plc has 1 FDA 510(k) cleared medical devices. Based in Llanelli, Carmarthenshire, GB.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Chromogenex Plc Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Chromogenex Plc
1 devices