FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

IU Implant System

K Number: K172345 · Decision Jun 18, 2018
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
320

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Basic Information

Device Name
IU Implant System
K Number
K172345
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Warantec Co., Ltd.
Date Received
August 2, 2017
Decision Date
June 18, 2018
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

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Other Clearances by Warantec Co., Ltd.

K Number Device Name
K221972 Warantec Custom Abutment
K221969 IU Implant System Abutment
K081748 ONEPLANT DENTAL IMPLANT SYSTEM