Refine USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Refine USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: Rejuvapen NXT
2
Total
2
Cleared
0
Denied
Refine USA, LLC has 2 FDA 510(k) cleared medical devices. Based in Jacksonville Beach, US.
Historical record: 2 cleared submissions from 2012 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Refine USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Technireg, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Refine USA, LLC
2 devices