Ceragem International, Inc. is one of 19028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ceragem International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CERAGEM AUTOMATIC THERMAL MASSAGER, LABONACHECK A1C, CERAGEM RH1 AUTOMATIC THERMAL MASSAGER
3
Total
3
Cleared
0
Denied
Ceragem International, Inc. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 2006 to 2014. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Ceragem International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ceragem International, Inc.
3 devices