Beacon Endoscopic is one of 15078 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beacon Endoscopic - FDA 510(k) Cleared Devices
Recent clearances: BNX DELIVERY SYSTEM PRE-LOADED WITH 19, 22 AND 25 GAUGE NEEDLE, 19, 22 OR 25 GAUGE NEEDLES (INDIVIDUALLY STERILE-PACKED,
1
Total
1
Cleared
0
Denied
Beacon Endoscopic has 1 FDA 510(k) cleared medical devices. Based in Auburndale, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Beacon Endoscopic Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beacon Endoscopic
1 devices