FDA UDI Not in Commercial Distribution 🇺🇸 United States

truSculpt

DI: 00816722021403 · Model: truSculpt · CUTERA, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
truSculpt
Primary DI
00816722021403
Version / Model
truSculpt
Company Name
CUTERA, INC.
Labeler DUNS
041071643
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2023-07-21
Public Version Status
Update
Public Device Record Key
16be0c7a-0146-452a-9f78-e0521d9e9afe
Distribution End Date
2019-12-31

Device Description

truSculpt RF Device

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
PBX Massager, Vacuum, Radio Frequency Induced Heat
NUV Massager, Vacuum, Light Induced Heating
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
45219 Radio-frequency skin contouring system

Identifiers

Type ID
Primary 00816722021403

Customer Contacts