Newmark, Inc. is one of 18407 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Newmark, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Painmaster MCT Patch, PAINMASTER MCT PATCH, PAINMASTER MCT PATCH
3
Total
3
Cleared
0
Denied
Newmark, Inc. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 2009 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Newmark, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Newmark, Inc.
3 devices