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FDA 510(k)

InMode System with vTone Applicator

K-Number: K200293 · 2020-05-05

ApplicantInMode , Ltd.
Decision Date2020-05-05
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

InMode System with vTone Applicator is the device name listed in this FDA 510(k) record. The listed applicant is InMode , Ltd.. It received FDA 510(k) clearance on 2020-05-05 under 510(k) number K200293. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InMode System with vTone Applicator?

InMode System with vTone Applicator is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is InMode , Ltd.. The 510(k) number is K200293.

When did InMode System with vTone Applicator receive FDA 510(k) clearance?

InMode System with vTone Applicator received FDA 510(k) clearance on 2020-05-05, under 510(k) number K200293.

Who is the listed applicant for InMode System with vTone Applicator?

The FDA 510(k) record lists InMode , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InMode System with vTone Applicator?

The FDA product code for InMode System with vTone Applicator is KPI.

Other records listing InMode , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: KPI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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