FDA UDI In Commercial Distribution 🇺🇸 United States

FAQ 102

DI: 07640260120112 · Model: Topaz · Foreo AB
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FAQ 102
Primary DI
07640260120112
Version / Model
Topaz
Company Name
Foreo AB
Labeler DUNS
352394143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-18
Public Version
2
Public Version Date
2025-06-30
Public Version Status
Update
Public Device Record Key
a7aee211-d588-4e6a-b321-24668c388f16

Device Description

FAQ™ 102 devices are over-the-counter home use devices intended for facial and neck skin stimulation, and non-invasive treatments of mild to moderate facial wrinkles for adult women with all skin tones.

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
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
PAY Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction
OHS Light Based Over The Counter Wrinkle Reduction

GMDN Terms

Code Name
45219 Radio-frequency skin/body contouring system

Identifiers

Type ID
Primary 07640260120112

Premarket Submissions

Submission Number Supplement Number
K240616 000