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

LAP-iX2N

K Number: K253165 · Decision Jun 9, 2026
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
9
Review Days
256

Basic Information

Device Name
LAP-iX2N
K Number
K253165
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
Sejong Medical Co., Ltd.
Date Received
September 26, 2025
Decision Date
June 9, 2026
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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K173112 LAP-iX
K171726 LapBag
K171741 Laport