Techen Safety, Inc. is one of 24282 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Techen Safety, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SEKURIT SHARPS COLLECTION CONTAINER
1
Total
1
Cleared
0
Denied
Techen Safety, Inc. has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Techen Safety, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Techen Safety, Inc.
1 devices