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CPMT Ares – Quadruple Laser System

Canadian Pioneer Medical Technology Corporation · Model CPMT Ares · UDI-DI 00199284314580

GEX

510(k) clearances

44,035

Adverse events (107 deaths)

201

Recalls

488

Facilities

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.

Recalls

Date	Firm	Reason
2026-08-06	Lutronic Corporation	Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.
2026-05-05	IPG Medical Corporation	Software anomaly that causes a false display of error code 5018.
2026-02-27	Olympus Corporation of the Americas	Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperabl
2026-02-27	Olympus Corporation of the Americas	Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperabl
2026-01-27	Lutronic Corporation	Reports of devices sparking/popping and potentially burning patients.
2025-12-15	LEASEIR TECHNOLOGIES SLU	The console label for affected devices is missing the "DANGER" symbol.
2025-07-22	LUMENIS, LTD.	The potential for unsterilized product within finished product labeled as sterile.
2025-05-06	Olympus Corporation of the Americas	Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or
2025-05-06	Olympus Corporation of the Americas	Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or
2025-05-06	Olympus Corporation of the Americas	Potential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.