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FDA 510(k)

InMode RF Multi-System

K-Number: K201150 · 2020-07-22

ApplicantInMode , Ltd.
Decision Date2020-07-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

InMode RF Multi-System is a medical device manufactured by InMode , Ltd.. It received FDA 510(k) clearance on 2020-07-22 under approval number K201150. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InMode RF Multi-System?

InMode RF Multi-System is a medical device that received FDA 510(k) clearance on 2020-07-22. It is manufactured by InMode , Ltd.. The 510(k) number is K201150.

When was InMode RF Multi-System approved by the FDA?

InMode RF Multi-System received FDA 510(k) clearance on 2020-07-22, under approval number K201150.

What company makes InMode RF Multi-System?

InMode RF Multi-System is manufactured by InMode , Ltd..

What is the FDA product code for InMode RF Multi-System?

The FDA product code for InMode RF Multi-System is GEI.

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Related PubMed Literature

PMID: 42168293 Comparative in vitro and in vivo assessment of three experimental extracellular matrix meshes for soft tissue remodeling. Scientific reports (2026)

Other Devices by InMode , Ltd.

K192249InMode System with Tone Applicator K200947InMode System with the Morhpeus8 Applicators K200293InMode System with vTone Applicator K210877Evolve System with the T3 Applicator K201285InMode Evolve System with the Tone Applicator K221571InMode Multi-system

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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