Identity
- Trade Name
- CPMT Ares – Quadruple Laser System FDA UDI
- Generic Name
- General/multiple surgical frequency-doubled solid-state laser system FDA UDI
- Device Name
- CPMT Ares is a quadruple-wavelength semiconductor laser system featuring four separate handpieces: 755 nm Alexandrite, 808 nm Diode, 1064 nm Nd:YAG, and a combined triple-wavelength handpiece (755, 808, and 1064 nm). It is intended for permanent hair removal on all skin types, treatment of vascular lesions such as spider veins and angiomas, pigmented lesions such as freckles and melasma, and overall skin rejuvenation. The system provides high-tech skin cooling, adjustable fluence, pulse duration, and multiple spot sizes to enhance safety and treatment precision. CPMT Ares is used in dermatology clinics, aesthetic centers, and medical spas. The device complies with applicable international standards for laser safety and performance. FDA UDI
- Model / Reference
- CPMT Ares FDA UDI
- Description
- CPMT Ares is a quadruple-wavelength semiconductor laser system featuring four separate handpieces: 755 nm Alexandrite, 808 nm Diode, 1064 nm Nd:YAG, and a combined triple-wavelength handpiece (755, 808, and 1064 nm). It is intended for permanent hair removal on all skin types, treatment of vascular lesions such as spider veins and angiomas, pigmented lesions such as freckles and melasma, and overall skin rejuvenation. The system provides high-tech skin cooling, adjustable fluence, pulse duration, and multiple spot sizes to enhance safety and treatment precision. CPMT Ares is used in dermatology clinics, aesthetic centers, and medical spas. The device complies with applicable international standards for laser safety and performance. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00199284314580 FDA UDI
- 510(k) Number
- K222915 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- General/multiple surgical frequency-doubled solid-state laser system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
No
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: General/multiple surgical frequency-doubled solid-state laser system
CPMT Ares – Quadruple Laser System by Canadian Pioneer Medical Technology Corporation — 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
- Canadian Pioneer Medical Technology Corporation
Sources (1)
- FDA UDI 95e0c678-e8c7-4119-9086-5eb17d3b1c84 34 fields · synced Jun 8, 2026