Medbio, LLC is one of 18492 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medbio, LLC - FDA 510(k) Cleared Devices
Recent clearances: Medifine Pen Needle 3 Bevel, Medifine Pen Needle Quinta 5 Bevel
1
Total
1
Cleared
0
Denied
Medbio, LLC has 1 FDA 510(k) cleared medical devices. Based in Cooper City, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medbio, 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 - Medbio, LLC
1 devices