Bicon, Inc.
Bicon, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2006.
Top product codes for Bicon, Inc.
Recent clearances by Bicon, Inc.
- K062044 — THE 5.0 X 6.0MM DENTAL IMPLANT
- K051091 — SYNTHOGRAFT
- K050712 — 4.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANT
- K050408 — BICON ORTHODONTIC IMPLANT SYSTEM
- K031568 — BICONITE SURFACE TREATMENT
- K042637 — THE 5.0 X 6.0MM DENTAL IMPLANT
- K023705 — BICON TRANSITIONAL IMPLANT (BTI) SYSTEM
- K010185 — 6.0 X 5.7MM DENTAL IMPLANT
- K994037 — THE 4.5MM DIAMETER BICON DENTAL IMPLANT
- K982488 — BICON BONE SCREW SYSTEM
- K973056 — BONE GRAFT SCREW SYSTEM
- K972417 — THE 6.0 X 8.0MM DENTAL IMPLANT SYSTEM
- K972029 — BICON DENTAL IMPLANTS II PART ABUTMENT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.