Chromogenex Technologies, Ltd. is one of 482 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Chromogenex Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V)
1
Total
1
Cleared
0
Denied
Chromogenex Technologies, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Llanelli, Carmarthenshire, GB.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Chromogenex Technologies, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chromogenex Technologies, Ltd.
1 devices