FDA 510(k) Applications Submitted by BICON, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K972029 |
06/02/1997 |
BICON DENTAL IMPLANTS II PART ABUTMENT SYSTEM |
BICON, INC. |
K010185 |
01/19/2001 |
6.0 X 5.7MM DENTAL IMPLANT |
BICON, INC. |
K050408 |
02/17/2005 |
BICON ORTHODONTIC IMPLANT SYSTEM |
BICON, INC. |
K050712 |
03/17/2005 |
4.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANT |
BICON, INC. |
K051091 |
04/28/2005 |
SYNTHOGRAFT |
BICON, INC. |
K031568 |
05/20/2003 |
BICONITE SURFACE TREATMENT |
BICON, INC. |
K972417 |
06/27/1997 |
THE 6.0 X 8.0MM DENTAL IMPLANT SYSTEM |
BICON, INC. |
K982488 |
07/17/1998 |
BICON BONE SCREW SYSTEM |
BICON, INC. |
K062044 |
07/19/2006 |
THE 5.0 X 6.0MM DENTAL IMPLANT |
BICON, INC. |
K973056 |
08/15/1997 |
BONE GRAFT SCREW SYSTEM |
BICON, INC. |
K042637 |
09/27/2004 |
THE 5.0 X 6.0MM DENTAL IMPLANT |
BICON, INC. |
K023705 |
11/04/2002 |
BICON TRANSITIONAL IMPLANT (BTI) SYSTEM |
BICON, INC. |
K994037 |
11/29/1999 |
THE 4.5MM DIAMETER BICON DENTAL IMPLANT |
BICON, INC. |
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