The Luminance RED Acne Device
Summary
Luminance Medical Ventures, Inc. received 510(k) clearance for The Luminance RED Acne Device, a OLP device. Cleared on 2022-06-09.
Details
Source
510(k) Clearance
External ID
K220729
Action Date
2022-06-09
Status
Traditional
Category
device
Product Code
OLP
Product Description
The Luminance RED Acne Device. Product code: OLP.
Context & Analysis
A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Luminance Medical Ventures, Inc. has received 2 total clearances in our database.
Luminance Medical Ventures, Inc. has 2 FDA actions in our database, including 2 clearances.
Frequently Asked Questions
What does 510(k) clearance mean?
A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.
How often does Luminance Medical Ventures, Inc. have FDA actions?
Luminance Medical Ventures, Inc. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K220729" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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