Medical Device Manufacturer · US , Boston , MA

Bicon, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1997

Recent clearances: BICON BONE SCREW SYSTEM, BONE GRAFT SCREW SYSTEM, THE 6.0 X 8.0MM DENTAL IMPLANT SYSTEM

13

Total

13

Cleared

0

Denied

FDA 510(k) Regulatory Record - Bicon, Inc. Dental ✕

13 devices

1-12 of 13

Cleared Nov 21, 2006

THE 5.0 X 6.0MM DENTAL IMPLANT

Cleared Sep 01, 2005

Cleared Apr 22, 2005

4.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANT

Cleared Apr 07, 2005

BICON ORTHODONTIC IMPLANT SYSTEM

Cleared Nov 23, 2004

BICONITE SURFACE TREATMENT

Cleared Nov 15, 2004

THE 5.0 X 6.0MM DENTAL IMPLANT

Cleared Jan 29, 2003

BICON TRANSITIONAL IMPLANT (BTI) SYSTEM

Cleared Dec 30, 2002

6.0 X 5.7MM DENTAL IMPLANT

Cleared Jan 11, 2000

THE 4.5MM DIAMETER BICON DENTAL IMPLANT

Cleared Jan 26, 1999

BICON BONE SCREW SYSTEM

Cleared Nov 12, 1997

BONE GRAFT SCREW SYSTEM

Cleared Sep 17, 1997

THE 6.0 X 8.0MM DENTAL IMPLANT SYSTEM