Manuals+

InLight 6/Port Controller & 2/Port Controller Owners Instruction Manual

Please read before using device.

Welcome

Thank you for choosing InLight(iL). iL products are engineered for safe, non-invasive, and effective use in clinical and home environments. Thousands of families are currently enjoying the benefits of light therapy.

Medical health providers use light therapy in clinical settings to increase circulation, reduce pain and, as research evidence demonstrates, to promote wound healing. iL products produce a gentle heat and do not require constant monitoring making it safe for patient home use.

FDA CLEARED Benefits:

Polychromatic Light Therapy

iL products contain visible 450nm blue diodes, 650nm red diodes, and infrared light diodes that range from 880nm to 930nm, averaging 880nm, thereby penetrating at various depths and stimulating increased circulation through a broad range of tissue types.

Diagram illustrating polychromatic light therapy. It shows a spectrum from 400nm ultra violet to 880nm infrared, with corresponding wavelengths (400nm ultra violet, 450nm blue, 500nm cyan, 550nm green, 600nm yellow, 650nm red, 880nm infrared). It depicts penetration depths into skin layers: Epidermis (2-3mm), Dermis (8-10mm), and Subcutaneous Layer (20-100mm).

Pad Systems

iL products are impregnated with super luminous diodes designed specifically and exclusively for our products. The circuitry architecture embedded in the neoprene allows for pliability and comfortable application of the pads to any body part.

This contoured application increases the skin absorption of the therapeutic light and enhances the benefits of each treatment session. The entire range of iL pads can be used interchangeably with any of our controller devices.

Image of a person's foot and ankle being treated with an InLight pad, and another image of a woman receiving treatment on her arm with a pad.

? Mitochondria: Specialized structures in each cell responsible for creating ATP, the energy molecule that fuels all cellular activity.

? Near-Infrared Light (NIR): Refers to the use of infrared light applied directly to living tissue.

? Nitric Oxide (NO): A chemical molecule released from the body under the influence of polychromatic light therapy.

? Polychromatic Light Therapy (PLT): The use of two or more LED light wavelengths (colors) to affect biologic changes.

? Wavelength: The length in nanometers of each color on the visible and invisible light spectrum.

NOTE: Controllers like the 2/PORT shown above feature multiple input ports for up to 2 pads working simultaneously.

NOTE: Controllers like the 6/PORT PRO shown above feature multiple input ports for up to 6 pads working simultaneously.

Parts Checklist

Caring for Your System

Indications for Use

1) To provide LED (light-emitting diode) light-associated gentle warmth (limited temperature elevation) therapy to temporarily relieve minor pain, stiffness and muscle spasms; and

2) To temporarily increase the local blood circulation of body parts.

Contraindications

Precautions

Electrical Considerations

Other Considerations

? Frequency: The rate at which photon energy (information) is delivered. (e.g. duty cycle, pulsed rate). Cellular and DNA communication can be measured in frequencies.

? Joules (j): A measurement of energy transfer.

? Laser Therapy: High-density light devices used for ablation, cutting and thermal coagulation of tissue.

Image of a woman smiling while receiving light therapy treatment on her neck with an InLight pad.

Device Set-up & Operation

The 2/Port Controller

Image of the 2-Port controller with labels for SETTING, POWER, ON, OFF buttons.

• Insert the power cable into 110-volt power outlet.

• Insert power supply jack into the InLight controller power jack (see picture below).

Image of the controller power jack with multiple DIN sockets.

• Connect the pad(s) to the controller at the top of the unit using any or all DIN sockets.

• Place the pad(s) with the LED side of light array on the treatment area.

• Press the [Power Button] button to initiate treatment.

Operation Modes

The 2/PORT Controller has 2 user buttons:

The 6/Port Controller

Image of the 6-Port PRO controller with labels for ON/OFF, START/STOP, SETTING, SOUND MUTE buttons.

• Insert the power cable into 110-volt power outlet.

• Insert power supply jack into the InLight controller power jack.

Image of the controller power jack with multiple DIN sockets.

• Connect the pad(s) to the controller at the top of the unit using any or all DIN sockets.

• Place the pad(s) with the LED side of light array on the treatment area.

• Press the [Power Button] button to initiate treatment.

Operation Modes

The 6/PORT Controller has 4 user buttons:

Notes on LED Usage

? NOTE: Please note every other row of LEDs are infrared and cannot be seen with the human eye. If the red LEDs are illuminated, the infrared LEDs will also be powered but you will not be able to see them.

? NOTE: Be aware lying directly on the pad(s) results in the lack of airflow and may result in elevated warmth in the area.

Images showing InLight logo in blue and red light.

Choosing a Setting

To use a different automatic or manual mode, press the [Setting Button] button until the desired LED indicator is illuminated. The unit will operate on that setting until it powers off. The unit will switch off automatically after 20 minutes in any mode.

Collage of images showing InLight pads applied to different body parts (face, arm, shoulder, neck).

? Near infrared light (NIR): Refers to the use of infrared light applied directly to living tissue.

? Nitric Oxide (NO): A chemical molecule released from smooth muscle when triggered by the body's parasympathetic response and/or polychromatic light therapy.

? Wavelength: The length in nanometers of each color on the visible and invisible light spectrum.

Suggested Application Guidelines

The standard treatment protocol for application is twice a day for 20 minutes per session as follows:

Remember, increasing circulation triggers physiologic responses that can last for hours or days. As such, some conditions may be adequately treated with 10-minute sessions three (3) times per week. In all cases, follow the direction of your healthcare provider.

Important Notice

EXPECTED SERVICE LIFE: 1 Year Under Warranty, Repairs Available for the Lifetime of the Device. Manufacturing Date Documented On Each Pad And Controller.

? IMPORTANT NOTICE

If any part of the InLight product fails or unit is not working you should contact InLight at 888-455-4116 or by email at repairs@inlighttherapyco.com for a return and repair authorization form.

⚠️ Do not attempt to fix the unit, in case of any failure as this will void your warranty.

Opening the control unit may cause an electrical shock if certain components are touched.

Opening the control unit or pads will void the warranty.

Only use iL approved and provided accessories with all InLight equipment. Failure to do so may result in damage to equipment, and cause health, fire, and/or safety problems.

Warranty Information

InLight warrants each new device to be free from defects in materials and workmanship for a period of one (1) year. The obligation of InLight under this warranty is expressly, solely and exclusively limited to the repair or replacement for the unit(s) or any parts thereof, which to the satisfaction of InLight, shall have become defective during the warranty period. This warranty does not extend to any liability to medical expenses or for any other direct, indirect or consequential damages caused by failure, defect or malfunction of any InLight product, except as herein provided.

This warranty shall not apply to any InLight product that has been repaired, tampered with or altered by someone other than a duly authorized InLight representative, or that has not been used in accordance with the enclosed instructions or stated purpose. All accessories used with a InLight product must be provided by InLight or authorized representative including, but not limited to, the power supply and securing straps. If items of this nature not provided by InLight or an authorized representative, are used with an InLight system, this warranty will be voided. Additionally, InLight will not be held liable for any mishaps relating to the InLight product. This warranty is warranted by InLight and is deemed to be the only warranty honored by InLight in lieu of any and all warranties expressed or provided by any and all other merchants, distributors, companies or persons. No person or entity has any authority to bind any InLight product to any warranty or guarantee except as specifically set forth herein.

Defective InLight equipment must be returned to InLight.

InLight disclaims all other warranties, either express or implied, including but not limited to implied warranties relating to the use of the product and/or result from the use of the product and any warranties which may be implied as a result of the purpose for which the product was manufactured. Not every person may obtain desired results from the use of any InLight product. In no event will InLight be held responsible or liable for any failure to produce claimed results arising out of the use or non-use of any InLight product.

? Photobiomodulation: Light changes biology.

? Photon: A wave or a particle representing light having no mass. Photons transmit information measured in frequencies within and between cells.

Recommendations for Training

None required to operate this device.

Caring for Your System

Disinfect the non-porous pads regularly with hospital grade disinfectant solution (1:10 bleach solution). Spray onto a cloth and lightly wipe clean with cloth. Do not soak or saturate. Do not autoclave.

Image of a person cleaning an InLight pad with a cloth and disinfectant spray.

Image of a foot wrapped in a pad and plastic bag.

Keep pads clean by always covering treatment area or pads with a clear plastic barrier such as plastic wrap or clear bags for the foot and/or open wounds. InLight suggests using 10 x 30" 1 Mil Poly Bags available through www.uline.com - model# S-10890.

? Coherent Light: Emitted by laser devices in a single, columnar form.

? Non-coherent light: Delivered by light emitting diodes (LED) via hands off devices safe for home use.

? Lumen: A measure of the total amount of visible light emitted by a source.

? Mitochondria: Specialized structures in each cell responsible for creating ATP, the energy molecule that fuels all cellular activity, and much more. [Source: UMDF.org]

Storage Instructions

Store in a cool, dry place, within the temperature ranges of 32-110°F.

A 35-Year History with Light

Recognizing need is a catalyst for inspiration. Following inspiration through to invention requires commitment, focus and passion. Each advance implemented is a result of identifying one solution born of a multitude of ideas. This is the process of innovation; And innovation takes time.

At InLight innovation has taken us on a 35-year journey. We have committed our careers, our family and our lives to creating the finest LED light therapy technology in any marketplace. We've committed ourselves to innovation.

Image displaying the range of InLight LED therapy pads and controllers.

Our Mission

Design, manufacture, and deliver the finest LED Light Energy systems in any marketplace while supporting our distribution network and serving our customers with consistency, integrity, and respect.

Technical Description

Symbol Key

Symbol Description
? Read usage instructions
⚠️ Caution, consult documents
? Serial number
[Manufacturer icon] Manufacturer
[Calendar icon] Manufacturing date
[Type B icon] Type B Applied Part
[Umbrella icon] Protection from rain
[Thermometer icon] Temperature limitation
▶️ On
⏹️ Off
? On/Off (push-push)

Model Type: 6/Port Controller System, 2/Port Controller System

Device/System Parts Include: iL 6 Port Controller / 2/Port Controller System and iL Power Supply (OUTPUT: 12.0V-5.0A). The power supply can be considered as the disconnection from the MAINS.

Applied Parts Include: Flexible Light Therapy Pads. The following pads are interchangeable for use - BODY/264, LOCAL/132, FACEMASK/104, SPINAL/112, BOOT/122, SMALL/50, PAINBUSTER/90, PAINBUSTER II/180, SPORTS/180.

Accessories Include: Protective Eyewear

This device does not require professional installation by service personnel. Manufacturer will provide circuit diagrams, component part lists, descriptions and instructions to assist Service Personnel in all requested parts repairs. This system, subject to mechanical wear, electrical, environmental degradation or aging is accessible for inspection, replacement and maintenance.

WARNING: Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.

WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment should be observed to verify that they are operating normally.

WARNING: Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30cm (12 inches) to any part of the InLight device, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put in service according to the EMC information in the Electromagnetic Capability of this manual.

Guidance and manufacturer's declaration - electromagnetic emissions

The In Light Wellness Systems (ILWS) Micro and 6/Port are intended for use in the electromagnetic environment specified below. The customer or the user of the Micro or 6/Port should assure that it is used in such an environment.

Emissions Test Compliance Group Electromagnetic environment - guidance
RF emissions CISPR 11 Group 1 The Micro and 6/Port use RF energy only for their internal function. Therefore, their RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
RF emissions CISPR 11 Class A The Micro and 6/Port are suitable for use in all establishments other than domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions IEC 61000-3-2 Class A
Voltage fluctuations/ flicker emissions Complies

Guidance and manufacturer's declaration - electromagnetic immunity

The Micro and 6/Port are intended for use in the electromagnetic environment specified below. The customer or the user of Micro or 6/Port should assure that it is used in such an environment.

IMMUNITY test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Electrostatic discharge (ESD) IEC 61000-4-2 ± 6 kV contact
± 8 kV air		 ± 6 kV contact
± 8 kV air		 Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.
Electrical fast transient/burst IEC 61000-4-4 ± 2 kV for power supply lines
±1 kV for input/output lines		 ± 2 kV for power supply lines
±1 kV for input/output lines		 Mains power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5 + 1 kV line(s) to line(s)
+ 2 kV line(s) to earth		 + 1 kV line(s) to line(s)
+ 2 kV line(s) to earth		 Mains power quality should be that of a typical commercial or hospital environment.
Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 <5% UT
(>95% dip in UT) for 0,5 cycle
40% UT
(60% dip in UT) for 5 cycles
70% UT
(30% dip in UT) for 25 cycles
<5% UT
(>95% dip in UT) for 5 s		 <5% UT
(>95% dip in UT) for 0,5 cycle
40% UT
(60% dip in UT) for 5 cycles
70% UT
(30% dip in UT) for 25 cycles
<5% UT
(>95% dip in UT) for 5 s		 Mains power quality should be that of a typical commercial or hospital environment. If the user of the Micro or 6/Port requires continued operation during power mains interruptions, it is recommended that the Micro or 6/Port be powered from an uninterruptible power supply or a battery.
Power frequency (50/60 Hz) magnetic field 3 A/m 3 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

NOTE: UT is the a.c. mains voltage prior to application of the test level.

Guidance and MANUFACTURER'S declaration - electromagnetic immunity

The In Light Wellness Systems (ILWS) Micro and 6/Port are intended for use in the electromagnetic environment specified below. The customer or the user of the Micro or 6/Port should assure that it is used in such an environment.

Immunity test IEC 60601 TEST LEVEL Compliance level Electromagnetic environment - guidance
Conducted RF IEC 61000-4-6 3 Vrms
150 kHz to 80 MHz		 3 Vrms Portable and mobile RF communications equipment should be used no closer to any part of the Micro or 6/Port Controller, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.
Radiated RF IEC 61000-4-3 3 V/m
80 MHz to 2,5 GHz		 3 V/m Recommended separation distance
d = 1.2 √P (150 kHz to 80 MHz)
d = 1.2 √P (80 MHz to 800 MHz)
d=2.3 √P (800 MHz to 2.5 GHz)
Where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).
Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range.b
Interference may occur in the vicinity of equipment marked with the following symbol: ((()))

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the Micro or 6/Port is used exceeds the applicable RF compliance level above, the Micro or 6/Port should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the Micro or 6/Port.

b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

Recommended separation distances between portable and mobile RF communications equipment and the Models Micro and 6/Port

The models Micro and 6/Port are intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Micro or 6/Port can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Micro or 6/Port as recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of transmitter (W) Separation distance according to frequency of transmitter (m)
150 kHz to 80 MHz
d = 1.17 √P		 80 MHz to 800 MHz
d = 1.17 √P		 800 MHz to 2.5 GHz
d = 2.33 √P
0,01 0,12 0,12 0,23
0,1 0,37 0,37 0,74
1 1,17 1,17 2,33
10 3,69 3,69 7,37
100 11,67 11,67 23,33

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.

NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Device Description

Power: Output Power Increments - 12V DC, Output Port 5 Pin Din Jack, Power/Energy Range 100-240 VAC

Increments of Power: 10.4-12VDC

Energy of Power: 5-5Amps

Beam Diameter/Spot Size: 5mm

Delivery System: Light Emitting Diodes

Wave Length: 430nm – 880nm

Controls: Push button

Patient Contacting Materials: Neoprene, plastic diode casing

Temperature at user skin surface: 100-124°F

Storage Temperature: 32-110°F

Recommended distance from patient: Contact skin

Timer Modes: 20 minutes

Weight: Varies per pad and controller

Dimensions: Varies per pad and controller

Intended Operator Language: English (US)

Manual Version Identifier: IL6/PORT2/PORTRXv721

Have Questions?

WE ARE HERE TO HELP INLIGHTEN YOU!

Legally marketed as a Class II Medical Device under FDA indications for use to temporarily relieve minor pain, stiffness and muscle spasms; and to temporarily increase local blood circulation.

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