Duns Number:514891048
Device Description: An over the counter device indicated to emit energy in the red and IR region of the spectr An over the counter device indicated to emit energy in the red and IR region of the spectrum for use in dermatology for the treatment of periorbital wrinkles.
Catalog Number
7290106259218
Brand Name
PREMIER (AVOLOGI)
Version/Model Number
Renelif
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OHS
Product Code Name
Light Based Over The Counter Wrinkle Reduction
Public Device Record Key
43c152ac-cb1d-49f8-9734-26b3e3f4e4f8
Public Version Date
November 16, 2020
Public Version Number
7
DI Record Publish Date
January 26, 2017
Package DI Number
27290106259212
Quantity per Package
6
Contains DI Package
17290106259215
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 14 |