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FDA 510(k)

reVive Perioral

K-Number: K172662 · 2018-01-09

ApplicantLed Technologies, Inc.
Decision Date2018-01-09
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

reVive Perioral is a medical device manufactured by Led Technologies, Inc.. It received FDA 510(k) clearance on 2018-01-09 under approval number K172662. 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 Perioral?

reVive Perioral is a medical device that received FDA 510(k) clearance on 2018-01-09. It is manufactured by Led Technologies, Inc.. The 510(k) number is K172662.

When was reVive Perioral approved by the FDA?

reVive Perioral received FDA 510(k) clearance on 2018-01-09, under approval number K172662.

What company makes reVive Perioral?

reVive Perioral is manufactured by Led Technologies, Inc..

What is the FDA product code for reVive Perioral?

The FDA product code for reVive Perioral is 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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