FDA UDI In Commercial Distribution 🇺🇸 United States

BEAR™

DI: 07350120790118 · Model: MINT · Foreo AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BEAR™
Primary DI
07350120790118
Version / Model
MINT
Company Name
Foreo AB
Labeler DUNS
352394143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-26
Public Version
2
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
db1cd87e-b7d1-4950-afbc-9f70cf069eba

Device Description

BEAR™ is intended for facial and neck stimulation and is indicated for over-the-counter cosmetic use. BEAR™ is a smart microcurrent facial toning device.

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
No
Has Lot/Batch Number
Yes
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

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Primary 07350120790118

Premarket Submissions

Submission Number Supplement Number
K200803 000