Red Light Therapy Device RL450MAX

Who This Device Is Typically Used By

The RL450MAX is commonly selected by larger clinics, multidisciplinary practices, and facilities offering full-body or large-area light exposure within structured wellness or recovery programs.

This model is often used in environments where space allows for wall-mounted or standing configurations and where multiple practitioners may share access to a high-output panel throughout the day.

Class II Medical Device
Distributed through a licensed Canadian Medical Device Establishment (MDEL #28304)

The RL450MAX is a professionally built red and near-infrared light therapy panel designed for use in controlled professional environments. It delivers targeted red and near-infrared light exposure as part of general wellness and recovery-focused applications.

Built for clinics, wellness facilities, and professional operators, the RL450MAX supports consistent, repeatable use in shared environments where durability, reliability, and operational clarity matter.

Professional Use Context

The RL450MAX is commonly integrated into professional wellness and recovery settings where non-invasive, light-based modalities are used alongside existing services. Its large treatment surface and high output make it suitable for full-body or large-area applications within structured programs.

Use of this device should always align with professional judgment, facility protocols, and the applicable scope of practice.

Technical Specifications

LED Count
450 LEDs (Red and Near-Infrared)

Dimensions
1200 × 300 × 65 mm

Weight
18.4 kg

Wavelengths
660 nm (Red)
850 nm (Near-Infrared)

Irradiance
Up to 300 mW/cm² at 12–18 inches

Treatment Duration
10–30 minutes per session

Power
AC 100–240V input
DC 36V output

What’s Included

RL450MAX panel
Power supply
Mounting hardware
Protective eyewear
User documentation

Regulatory & Distribution Information

The RL450MAX is distributed in Canada by Garnet Red Light under Aegis & Pulse Medical Supply Inc., a licensed Medical Device Establishment (MDEL #28304).

All devices are distributed in accordance with the manufacturer’s labeling, documentation, and applicable Canadian Medical Devices Regulations.