Uweport, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Uweport, LLC - FDA 510(k) Cleared Devices
Recent clearances: Powder free Nitrile Examination Glove-(Test for use with Chemotherapy Drugs)
1
Total
1
Cleared
0
Denied
Uweport, LLC has 1 FDA 510(k) cleared medical devices. Based in Charlotte, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Uweport, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Uweport, LLC
1 devices