510(k) K242386

Device
Bluemoon
Applicant
Genoss Co., Ltd.
510(k) number
K242386
Product code
EBZ
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-05
Date received
2024-08-12
Regulation
872.6070
Classification name
Activator, Ultraviolet, For Polymerization
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Jiyeon Lee
Address
12f, 76, Changnyong-Daero 256beon-Gil, Yeongtong-Gu Manufacturing Site: 3f, 4f, 5f, D-Factory, 56, Changnyong-Da Suwon-Si CN

FDA Registration Numbers

Source Documents

510(k) summary PDF

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