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.
Powerful. Precise.
NovoTHOR handles 2.7kW1Â 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.
2.7kW

Power
Advanced

Light engines
Dual

Cooling
Active

Treatment
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.
Medical Grade
Power Supply
Medical Grade

Safety Features
Low EM/RF

Interference
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.
James Carroll talking to engineer in Vermont, USA
Engineers talking about the high quality components that go into 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 | Length: 82.7 inches / 210 cm Depth: 38 inches / 96 cm
 Height: 36.6 inches / 93 cm Weight: 466 lbs / 211.5 kg |
Length: 94 inches / 238 cm Depth: 38 inches / 96 cm
 Height: 36.6 inches / 93 cm
 Weight: 4521.4 lbs  / 236.5 kg |
| Wavelength | Can be switched between red only and mixed red + near-infrared
 Red: 660nm
Near-infrared: 850nm |
Can be switched between red only and mixed red + near-infrared
 Red: 660nm
Near-infrared: 850nm |
| Power Requirement | TDP: 2,400 W
 Outlet: 220–240 VAC Maximum Current: 13A |
TDP: 2,400 W
 Outlet: 220–240 VAC Maximum Current: 13A |
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
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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 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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