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

ZENEX FreeMilling & CCM Cast Abutment

K Number: K231557 · Decision Aug 24, 2023
Classifications
1
FEI Numbers
382
Registration Numbers
382
Same Product Code
708
Applicant Total
8
Review Days
86

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Basic Information

Device Name
ZENEX FreeMilling & CCM Cast Abutment
K Number
K231557
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3630
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Izenimplant Co., Ltd.
Date Received
May 30, 2023
Decision Date
August 24, 2023
Product Code
NHA
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
NHA Abutment, Implant, Dental, Endosseous

Similar 510(k) Clearances

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Other Clearances by Izenimplant Co., Ltd.

K Number Device Name
K253334 ZENEX Implant System_Short (R-System)
K252585 ZENEX Implant System_R-System
K240560 ZENEX Implant System_Long
K232170 Ti Link Abutment
K233163 ZENEX Implant System_Short
K230630 ZENEX Implant System_Narrow
K211090 ZENEX Implant System