Medibio USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medibio USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: Medifine Pen Needle 3 Bevel
1
Total
1
Cleared
0
Denied
Medibio USA, LLC has 1 FDA 510(k) cleared medical devices. Based in Cooper City, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medibio USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medibio USA, LLC
1 devices