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

SAVE GBR

K Number: K222367 · Decision Mar 23, 2023
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
79
Applicant Total
37
Review Days
230

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Basic Information

Device Name
SAVE GBR
K Number
K222367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4880
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dentis Co., Ltd.
Date Received
August 5, 2022
Decision Date
March 23, 2023
Product Code
DZL
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
DZL Screw, Fixation, Intraosseous

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K233544 MESHEET
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K230307 Dentis i-Clean System
K230246 Dentis s-Clean SQ-SL Narrow Implant System
K230523 s-Clean Link Abutment Narrow
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