Unisis Corp. is one of 18378 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unisis Corp. - FDA 510(k) Cleared Devices
Recent clearances: UNIEVER Disposable Epidural Anesthesia Needle, UNIEVER Disposable Nerve Blocked Needle, UNIEVER DISPOSABLE SPINAL ANESTHESIA NEEDLE
2
Total
2
Cleared
0
Denied
Unisis Corp. has 2 FDA 510(k) cleared medical devices. Based in Richardson, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Unisis Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ken Block Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Unisis Corp.
2 devices