Bicon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bicon, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Bicon, Inc. has 13 FDA 510(k) cleared dental devices. Based in Boston, US.
Historical record: 13 cleared submissions from 1997 to 2006.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bicon, Inc.
13 devices
Cleared
Nov 21, 2006
THE 5.0 X 6.0MM DENTAL IMPLANT
Dental
125d
Cleared
Sep 01, 2005
SYNTHOGRAFT
Dental
126d
Cleared
Apr 22, 2005
4.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANT
Dental
36d
Cleared
Apr 07, 2005
BICON ORTHODONTIC IMPLANT SYSTEM
Dental
49d
Cleared
Nov 23, 2004
BICONITE SURFACE TREATMENT
Dental
553d
Cleared
Nov 15, 2004
THE 5.0 X 6.0MM DENTAL IMPLANT
Dental
49d
Cleared
Jan 29, 2003
BICON TRANSITIONAL IMPLANT (BTI) SYSTEM
Dental
86d
Cleared
Dec 30, 2002
6.0 X 5.7MM DENTAL IMPLANT
Dental
710d
Cleared
Jan 11, 2000
THE 4.5MM DIAMETER BICON DENTAL IMPLANT
Dental
43d
Cleared
Jan 26, 1999
BICON BONE SCREW SYSTEM
Dental
193d
Cleared
Nov 12, 1997
BONE GRAFT SCREW SYSTEM
Dental
89d
Cleared
Sep 17, 1997
THE 6.0 X 8.0MM DENTAL IMPLANT SYSTEM
Dental
82d
Cleared
Aug 18, 1997
BICON DENTAL IMPLANTS II PART ABUTMENT SYSTEM
Dental
77d