FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Ignite RF System

K Number: K251254 · Decision Jan 15, 2026
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
267

Basic Information

Device Name
Ignite RF System
K Number
K251254
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
InMode , Ltd.
Date Received
April 23, 2025
Decision Date
January 15, 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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