Medical Device Manufacturer · US , Washington , DC

Newmark, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Total

Cleared

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.

Newmark, Inc. is one of 4753 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Newmark, Inc.

3 devices

1-3 of 3