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

Dentis SQ-SL AXEL Fixture

K Number: K253493 · Decision Mar 4, 2026
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
37
Review Days
128

Basic Information

Device Name
Dentis SQ-SL AXEL Fixture
K Number
K253493
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentis Co., Ltd.
Date Received
October 27, 2025
Decision Date
March 4, 2026
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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K233544 MESHEET
K230126 Dentis s-Clean Regular Abutment
K230307 Dentis i-Clean System
K230246 Dentis s-Clean SQ-SL Narrow Implant System
K230523 s-Clean Link Abutment Narrow
K230203 Dentis I-FIX Abutment
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