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Decades of commitment

Our long history and commitment has given us an unmatched understanding of every aspect of Red Light Therapy. This understanding has been poured into NovoTHOR®, creating a device that is completely unmatched for power, dose, and light distribution.

The NovoTHOR whole body light pod

Powerful. Precise.

NovoTHOR handles 2.7kW1 of power with ease, distributing the power to light engines and drivers that regulate power flow, keeping the precise amount of power to meet strict dosage requirements. A mixture of active and passive cooling keep the LEDs efficient and your customer cool.

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2.7kW
Power
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Advanced
Light engines
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Dual
Cooling
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Active
Treatment

1NovoTHOR XL, see technical specifications for more details.

Always Testing

Every component of a NovoTHOR is tested at multiple stages. We use a laboratory grade spectrophotometer to measure light output through a 24 hour burn in procedure, ensuring that every NovoTHOR meets our high standards for continual light output.

Built to medical specifications

NovoTHOR uses a medical grade power supply and high specification EMI/RFI reduction technology to reduce EM and RF noise — allowing it to be used in hospital and clinical settings without interfering with vital equipment.

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Medical Grade
Power Supply
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Medical Grade
Safety Features
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Low EM/RF
Interference
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Dose
Regulation System

Made in the USA

We manufacture the high-precision components and assemble the NovoTHOR in the United States. We collaborate with industry leading LED specialists to build a product that is both staggeringly powerful and has a constant light output that your team can rely on.

Maryellen Ammons talks about using NovoTHOR

James Carroll talking to engineer in Vermont, USA

Engineers talking about the high quality components that go into NovoTHOR

Engineers talking about the high quality components that go into NovoTHOR

Maryellen Ammons talks about using NovoTHOR

How NovoTHOR maintains a long lifespan by using cooler LEDs

RoHS Compliant

We partner with high quality manufacturers and suppliers to ensure our products don't contain toxins or hazardous materials.

Pb

Lead Free

Hg

Mercury Free

Cd

Cadmium Free

Cr6+

Hexavalent
Chromium Free

PBB

Full List Below

For full RoHS compliance we ensure that our devices do not contain lead, mercury, cadmium, hexavalent chromium, PBB, PBDE, DEHP, BBP, DBP, or DIBP.

Technical specifications

NovoTHOR is designed to last, using a strong steel chassis, high power LEDs and custom designed light engines and drivers.

NovoTHOR

NovoTHOR XL

Dimensions
NovoTHOR

Length: 82.7 inches / 210 cm
Depth: 38 inches / 96 cm
Height: 36.6 inches / 93 cm
Weight: 466 lbs / 211.5 kg

NovoTHOR XL

Length: 94 inches / 238 cm
Depth: 38 inches / 96 cm
Height: 36.6 inches / 93 cm
Weight: 4521.4 lbs  / 236.5 kg

Wavelength
NovoTHOR

Can be switched between red only and mixed red + near-infrared

Red: 660nm
Near-infrared: 850nm

NovoTHOR XL

Can be switched between red only and mixed red + near-infrared

Red: 660nm
Near-infrared: 850nm

Power requirements
NovoTHOR

TDP: 2,400 W
Outlet: 220–240 VAC
Maximum Current: 13A

NovoTHOR XL

TDP: 2,700 W
Outlet: 220–240 VAC
Maximum Current: 14A

Regulatory

NovoTHOR is a medical device, so it is built to both our own high standards as well as many international standards, both voluntary and mandatory. It is independantly tested and carries both a CE and a UL mark and is made to GMP standards. Here is a full list of the standards that our product is built to.

BS EN ISO 13485

Medical devices. Quality management systems. Requirements for regulatory purposes

IEC 60601-1

Medical electrical equipment. General requirements for basic safety and essential performance

IEC 60601-2-57

Medical electrical equipment. Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use

IEC 62471

Photobiological safety of lamps and lamp systems

IEC 62304

Medical device software. Software life-cycle processes

BS EN ISO 10993–1

Biological evaluation of medical devices. Evaluation and testing within a risk management process

IEC 60601–1–2

Medical electrical equipment. General requirements for basic safety and essential performance. Collateral standard. Electromagnetic compatibility. Requirements and tests.

BS EN ISO 15223-1

Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied

BS EN ISO 14971

Medical devices. Application of risk management to medical devices.

IEC 60601–1–6

Medical electrical equipment. General requirements for basic safety and essential performance. Collateral standard. Usability.

IEC 62366

Medical devices. Application of usability engineering to medical devices.

Restriction of Hazardous Substances Directive

Restriction of use of specific hazardous materials found in electrical and electronic products.

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