Nanowear, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nanowear, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SimpleSense-BP, SimpleSense-BP Software Application, SimpleSENSE Platform, SimpleSENSE
4
Total
4
Cleared
0
Denied
Nanowear, Inc. has 4 FDA 510(k) cleared medical devices. Based in Brooklyn, US.
Last cleared in 2023. Active since 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nanowear, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Graematter, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Nanowear, Inc.
4 devices