Bicon, LLC is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bicon, LLC - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Bicon, LLC has 5 FDA 510(k) cleared medical devices. Based in Boston, US.
Historical record: 5 cleared submissions from 2008 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bicon, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bicon, LLC
5 devices
Cleared
Jun 02, 2015
Fiber Disks and Blocks (TRINIA)
Dental
172d
Cleared
Mar 14, 2014
TRINIA
Dental
109d
Cleared
Oct 01, 2010
BICON DENTAL IMPLANT SYSTEM 3.0MM BICON DENTAL IMPLANT
Dental
92d
Cleared
Oct 15, 2009
BICON IMPLANTS WITH A 2.5MM INTERNAL CONNECTION
Dental
101d
Cleared
Oct 10, 2008
5.0 X 5.0MM DENTAL IMPLANT AND 6.0 X 5.0 DENTAL IMPLANT
Dental
315d