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FDA 510(k)

reVive Light Therapy LED Ultrasonic Wrinkle System

K-Number: K180445 · 2018-05-15

ApplicantLed Technologies, Inc.
Decision Date2018-05-15
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

reVive Light Therapy LED Ultrasonic Wrinkle System is a medical device manufactured by Led Technologies, Inc.. It received FDA 510(k) clearance on 2018-05-15 under approval number K180445. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the reVive Light Therapy LED Ultrasonic Wrinkle System?

reVive Light Therapy LED Ultrasonic Wrinkle System is a medical device that received FDA 510(k) clearance on 2018-05-15. It is manufactured by Led Technologies, Inc.. The 510(k) number is K180445.

When was reVive Light Therapy LED Ultrasonic Wrinkle System approved by the FDA?

reVive Light Therapy LED Ultrasonic Wrinkle System received FDA 510(k) clearance on 2018-05-15, under approval number K180445.

What company makes reVive Light Therapy LED Ultrasonic Wrinkle System?

reVive Light Therapy LED Ultrasonic Wrinkle System is manufactured by Led Technologies, Inc..

What is the FDA product code for reVive Light Therapy LED Ultrasonic Wrinkle System?

The FDA product code for reVive Light Therapy LED Ultrasonic Wrinkle System is OHS.

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Related PubMed Literature

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Other Devices by Led Technologies, Inc.

K171386dpl SpectraLite K171390dpl II Panel K180447reVive Light Therapy LED Cleansing System K180320dpl IIa Panel K172662reVive Perioral K183247dpl Faceware

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Related Devices (Code: OHS)

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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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