FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BICON ORTHODONTIC IMPLANT SYSTEM

K Number: K050408 · Decision Apr 7, 2005
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
13
Review Days
49

Basic Information

Device Name
BICON ORTHODONTIC IMPLANT SYSTEM
K Number
K050408
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BICON, INC.
Date Received
February 17, 2005
Decision Date
April 7, 2005
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

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K Number Device Name
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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
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