The Luminance RED Acne Device
K-Number: K220729 · 2022-06-09
Device Summary
Frequently Asked Questions
What is the The Luminance RED Acne Device?
The Luminance RED Acne Device is a medical device that received FDA 510(k) clearance on 2022-06-09. The listed applicant is Luminance Medical Ventures, Inc.. The 510(k) number is K220729.
When did The Luminance RED Acne Device receive FDA 510(k) clearance?
The Luminance RED Acne Device received FDA 510(k) clearance on 2022-06-09, under 510(k) number K220729.
Who is the listed applicant for The Luminance RED Acne Device?
The FDA 510(k) record lists Luminance Medical Ventures, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for The Luminance RED Acne Device?
The FDA product code for The Luminance RED Acne Device is OLP.
Other records listing Luminance Medical Ventures, 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: OLP)
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.