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

NEW DOUBLO 2.0

K Number: K251334 · Decision Sep 29, 2025
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
8
Review Days
152

Basic Information

Device Name
NEW DOUBLO 2.0
K Number
K251334
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hironic Co., Ltd.
Date Received
April 30, 2025
Decision Date
September 29, 2025
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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