FDA UDI In Commercial Distribution 🇺🇸 United States

FAQ 101

DI: 07640260120037 · Model: Amethyst · Foreo AB
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FAQ 101
Primary DI
07640260120037
Version / Model
Amethyst
Company Name
Foreo AB
Labeler DUNS
352394143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-01
Public Version
2
Public Version Date
2025-06-30
Public Version Status
Update
Public Device Record Key
1f6b005c-018b-44de-92ac-a9d918502791

Device Description

FAQ™ 101 device is an over-the-counter home use devices intended for non-invasive treatments of mild to moderate periorbital wrinkles for adult women who have Fitzpatrick skin types I-VI.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PAY Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction
OHS Light Based Over The Counter Wrinkle Reduction

GMDN Terms

Code Name
44832 Multi-modality skin/body contouring system

Identifiers

Type ID
Primary 07640260120037

Premarket Submissions

Submission Number Supplement Number
K222012 000