FDA 510(k) FDA class 1 Substantially Equivalent 🇰🇷 South Korea

TRAUS ENDO

K Number: K212043 · Decision Jun 24, 2022
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
18
Review Days
359

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Basic Information

Device Name
TRAUS ENDO
K Number
K212043
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Saeshin Precision Co., Ltd.
Date Received
June 30, 2021
Decision Date
June 24, 2022
Product Code
EKX
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
EKX Handpiece, Direct Drive, Ac-Powered

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K201292 TRAUS SIP20
K192561 TRAUS SUS20
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K181129 STRONG Dental Handpieces
K171436 STRONG Dental Handpieces
K151171 TRAUS SUS10
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