Nsite, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nsite, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NSite Scoliosis Assessment App
1
Total
1
Cleared
0
Denied
Nsite, Inc. has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Last cleared in 2023. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Nsite, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nsite, Inc.
1 devices