FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Bluemoon

K Number: K242386 · Decision May 5, 2025
Classifications
1
FEI Numbers
101
Registration Numbers
101
Same Product Code
213
Applicant Total
18
Review Days
266

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Basic Information

Device Name
Bluemoon
K Number
K242386
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6070
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genoss Co., Ltd.
Date Received
August 12, 2024
Decision Date
May 5, 2025
Product Code
EBZ
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
EBZ Activator, Ultraviolet, For Polymerization

Similar 510(k) Clearances

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Other Clearances by Genoss Co., Ltd.

K Number Device Name
K222688 The Trust
K233885 rainbow Paste Stain SE
K232174 rainbowTM Multi-Layer Block / bright 3-Layer / bright Mono
K231480 Bright MTA Sealer Plus
K214086 Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite, Bright Impress-Putty
K200155 Bright High Flow
K200153 Bright Bond Universal
K200156 Bright Low Flow
K170596 TN-Brush
K160079 rainbow Shine
Search all 18 clearances from Genoss Co., Ltd. →