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

Tapered Pro Conical Implant System

K Number: K240187 · Decision Jun 5, 2024
Classifications
1
FEI Numbers
333
Registration Numbers
333
Same Product Code
1516
Applicant Total
3
Review Days
133

Basic Information

Device Name
Tapered Pro Conical Implant System
K Number
K240187
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BioHorizons Implant Systems Inc.
Date Received
January 24, 2024
Decision Date
June 5, 2024
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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Other Clearances by BioHorizons Implant Systems Inc.

K Number Device Name
K243521 Conical Ti Base abutments
K240531 SmartShape™ Healing Abutment; Wide Custom Milled Ti-Blank Abutment