Identity
- Trade Name
- Ultimate Contour Mini FDA UDI
- Generic Name
- Multi-modality skin/body contouring system FDA UDI
- Device Name
- Non-thermal radio frequency device for relief of minor aches and pains, relief of muscle spasms, temporary improvement in local circulation, and temporary reduction in the appearance of cellulite. FDA UDI
- Model / Reference
- 005-00036 FDA UDI
- Description
- Non-thermal radio frequency device for relief of minor aches and pains, relief of muscle spasms, temporary improvement in local circulation, and temporary reduction in the appearance of cellulite. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00872320004477 FDA UDI
- 510(k) Number
- K171052 FDA UDI
- FDA Product Code
- PBX FDA UDI
- GMDN Term
- Multi-modality skin/body contouring system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Multi-modality skin/body contouring system
Ultimate Contour Mini by Cao Group, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Cao Group, Inc.
Sources (1)
- FDA UDI 832ad484-e4ca-40ba-b313-47117e6bf8bf 35 fields · synced May 31, 2026