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

InMode RF System

K Number: K240780 · Decision Jul 24, 2024
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
15
Review Days
125

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
InMode RF System
K Number
K240780
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
March 21, 2024
Decision Date
July 24, 2024
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), ordered by most recent decision date.

View all

Other Clearances by InMode , Ltd.

K Number Device Name
K251254 Ignite RF System
K251632 Optimas MAX System
K242598 DEFINE System (AG612444A)
K240017 InMode System with the Morpheus8 90 Applicator
K233642 InMode RF System
K231495 The Evolve System with the Transform Applicator
K231790 The InMode System with the Morpheus8 Applicators
K221571 InMode Multi-system
K210877 Evolve System with the T3 Applicator
K201285 InMode Evolve System with the Tone Applicator
Search all 15 clearances from InMode , Ltd. →