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

EsFlow PLUS

K Number: K250317 · Decision May 30, 2025
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
17
Review Days
115

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Basic Information

Device Name
EsFlow PLUS
K Number
K250317
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spident Co., Ltd.
Date Received
February 4, 2025
Decision Date
May 30, 2025
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

Similar 510(k) Clearances

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Other Clearances by Spident Co., Ltd.

K Number Device Name
K250566 EsCem RMGI
K242702 VioSeal
K242675 FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37 5ml, FineEtch 37% 1.2ml 20ea pack)
K241445 K-Bond Universal
K231523 EsCom250
K214076 EsCem
K214071 Hexa-Temp
K161774 i-Sil
K134022 BASE IT
K134021 ESTEMP IMPLANT, ESTEMP CLEAR
Search all 17 clearances from Spident Co., Ltd. →