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

Dentis Dental Implant System

K Number: K150344 · Decision Jul 24, 2015
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
37
Review Days
163

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Basic Information

Device Name
Dentis Dental Implant System
K Number
K150344
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
February 11, 2015
Decision Date
July 24, 2015
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 Dentis Co., Ltd.

K Number Device Name
K253493 Dentis SQ-SL AXEL Fixture
K241065 ChecQ (AC100)
K233921 Luvis Chair (LC700C)
K241063 s-Clean ScanHealing Abutment
K240511 Dentis s-Clean SQ-SL Fixture
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
Search all 37 clearances from Dentis Co., Ltd. →