reVive Light Therapy LED Cleansing System
K-Number: K221430 · 2022-07-27
Device Summary
Frequently Asked Questions
What is the reVive Light Therapy LED Cleansing System?
reVive Light Therapy LED Cleansing System is a medical device that received FDA 510(k) clearance on 2022-07-27. The listed applicant is Led Technologies, Inc.. The 510(k) number is K221430.
When did reVive Light Therapy LED Cleansing System receive FDA 510(k) clearance?
reVive Light Therapy LED Cleansing System received FDA 510(k) clearance on 2022-07-27, under 510(k) number K221430.
Who is the listed applicant for reVive Light Therapy LED Cleansing System?
The FDA 510(k) record lists Led Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for reVive Light Therapy LED Cleansing System?
The FDA product code for reVive Light Therapy LED Cleansing System is OHS.
Other records listing Led Technologies, Inc. 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.
Related Devices (Code: OHS)
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.
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.