Biorenew Labs, LLC is one of 18413 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biorenew Labs, LLC - FDA 510(k) Cleared Devices
Recent clearances: SONILASE BLUE, SONILASE BLUE-CLEAN, SONILASE BLUE-UV CLEAN PLUS, SONILASE LIGHT THERAPY DEVICE
2
Total
2
Cleared
0
Denied
Biorenew Labs, LLC has 2 FDA 510(k) cleared medical devices. Based in Coralville, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biorenew Labs, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aegis Regulatory, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biorenew Labs, LLC
2 devices