Biolife, LLC is one of 21991 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biolife, LLC - FDA 510(k) Cleared Devices
Recent clearances: STATSEAL DISC, PRO QR ADVANCED FORMULA POWDER, PRO QR (QUICK RELIEF) POWDER (FOR MINOR EXTERNAL BLEEDING FROM WOUNDS & PROCEDURES)
3
Total
3
Cleared
0
Denied
Biolife, LLC has 3 FDA 510(k) cleared medical devices. Based in Sarasota, US.
Historical record: 3 cleared submissions from 2007 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Biolife, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biolife, LLC
3 devices