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

SMARTDent

K Number: K251109 · Decision May 21, 2025
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
24
Review Days
40

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Basic Information

Device Name
SMARTDent
K Number
K251109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ray Co., Ltd.
Date Received
April 11, 2025
Decision Date
May 21, 2025
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

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Other Clearances by Ray Co., Ltd.

K Number Device Name
K260462 RCT800
K251798 RCT700
K243903 RCT600
K233625 RAYDENT SW
K232325 RAYSCAN a-Expert
K232287 RAYSCAN a-Expert3D
K230753 RCT800
K213226 RCT700
K211105 Ear-Friendly Mask
K192737 RCT800
Search all 24 clearances from Ray Co., Ltd. →