What treatments is it suitable for?
The program selection provides starting points for adjunct treatment of arthrosis, knee osteoarthritis, knee pain, hip pain, ankle sprain, bursitis and other periarticular complaints.
Photobiomodulation can be used to influence pain and surrounding soft-tissue symptoms. It does not restore worn cartilage, meniscus or torn ligaments, and it does not replace physiotherapy, load modification or orthopaedic assessment.
Manufacturer protocols include acute and chronic back pain, lumbar and cervical syndromes, myofascial pain and complaints associated with radiculopathy.
Program names do not replace diagnosis. For radiating limb pain, muscle weakness, sensory disturbance, urinary or faecal dysfunction, trauma or rapid deterioration, medical assessment is required before treatment.
The program library may include protocols for shoulder pain, frozen shoulder, subacromial bursitis, rotator cuff-related complaints and post-operative rehabilitation.
Laser is an adjunct in rehabilitation. In cases of significant loss of strength, post-injury immobility or suspected complete tendon rupture, imaging and specialist assessment are necessary.
Epicondylitis, Achilles tendinopathy, patellar tendon complaints, De Quervain's syndrome, tenosynovitis and trigger point treatment are among the targeted areas listed in the source.
Tendon rehabilitation is based on load management and progressive strengthening. Pain reduction alone does not imply the tendon is ready for full sports or work loads.
For muscle pain, contracture, contusion, muscle strain, post-injury oedema and post-operative rehabilitation, laser can be part of a comprehensive treatment plan.
In acute injuries exclude fracture, complete rupture, infection and other urgent conditions first. High power is not intended to mask symptoms that prevent safe return to sport.
The plantar fasciitis program gives manufacturer starting points for targeted treatment of painful areas of the plantar fascia.
Laser does not remove a bony heel spur. Treatment aims to complement load management, appropriate footwear and rehabilitation by addressing surrounding soft-tissue complaints.
The program list includes oedema-management protocols related to acute injury and post-operative conditions.
Unknown-source swelling must be investigated first. Laser does not replace compression, mobilization, appropriate wound care or complex lymphoedema therapy.
Clinic use: The desktop format is advantageous in a dedicated treatment room, on a treatment trolley or a permanent workstation.
Why choose the PhysioLaser 6.0 Pro?
6 W maximum optical power
Its optical power matches the portable PhysioLaser 6.0 model. In maximum continuous mode up to 360 Joules per minute can be delivered.
85+ clinical protocols
The broad program library provides quick starting points for the most common musculoskeletal, sports rehabilitation and oedema-related treatments.
Desktop design for a fixed treatment site
The 220 × 170 × 60 mm, approximately 790 g central unit can be placed on a treatment trolley or a dedicated workspace.
Larger, 3-inch display
Compared with the portable 6.0 model's 2.6-inch display, the Pro offers a larger control surface for fixed clinic use.
11 mm base optics, 22 mm option
The package includes an 11 mm 808 nm treatment head. Larger optics and additional wavelength handpieces may be available as accessories.
Two protective goggles and emergency stop
Operator and patient goggles required for Class 4 treatment, plus a safety emergency stop, are included in the package.
Is the PhysioLaser 6.0 Pro right for you?
85+ built-in clinical protocols
The protocols listed in the source mainly cover musculoskeletal, sports rehabilitation and oedema-related treatments. Program selection simplifies setup but does not replace diagnosis, dose verification or treatment documentation.
Arthrosis, knee osteoarthritis, acute and chronic knee pain, hip pain, ankle sprain with oedema, bursitis, meniscal-related complaints, post-operative joint conditions and other manufacturer protocols.
The list summarizes the program groups given in the source. Exact program names and parameters should be verified in the device menu and user manual.
Acute and chronic back pain, lumbago, lumbar syndrome, radiculopathy-related back pain, spondylosis, myofascial back pain and post-operative complaints.
The list summarizes the program groups given in the source. Exact program names and parameters should be verified in the device menu and user manual.
Acute and chronic neck pain, cervical syndrome, myofascial neck pain, shoulder pain, frozen shoulder, rotator cuff-related complaints, bursitis and post-operative shoulder care.
The list summarizes the program groups given in the source. Exact program names and parameters should be verified in the device menu and user manual.
Epicondylitis, Achilles tendinopathy, patellar tendinopathy, De Quervain's syndrome, tenosynovitis, carpal tunnel syndrome, trigger points and plantar fasciitis.
The list summarizes the program groups given in the source. Exact program names and parameters should be verified in the device menu and user manual.
Oedema associated with acute injury, DOMS, muscle contracture, contusion, muscle strain, post-operative pain, rehabilitation phases, adjunct treatment in fibromyalgia and other sports medicine protocols.
The list summarizes the program groups given in the source. Exact program names and parameters should be verified in the device menu and user manual.
Optional handpieces: the standard package contains the 808 nm head. Availability, power, program compatibility and eye-protection requirements for 980 and 1064 nm heads must be verified separately.
What does 6 W laser treatment mean?
In photobiomodulation light of a defined wavelength and dose is delivered to the target tissue. The biological response depends on wavelength, power, energy dose, spot size, pulse settings and treatment geometry.
6 W maximum continuous power corresponds to 6 Joules per second, i.e. up to 360 Joules per minute. This allows rapid dose delivery but requires attention to tissue heating and avoiding excessive dose.
The standard 808 nm handpiece operates in the near-infrared range. Optional 980 and 1064 nm handpieces may offer different tissue absorption properties, but it is incorrect to simply rank them as “deeper” or automatically more effective.
Fixed placement can facilitate creating a consistent Class 4 safety environment, but this alone does not make the treatment safe.
Professional treatment in four steps
Assess the patient
Clarify diagnosis, treatment goal, tissue condition and contraindications. Program names are not a substitute for diagnosis.
Select the protocol and verify the dose
Check wavelength, power, mode, frequency, duty cycle, treatment time, spot size and treated area.
Ensure a Class 4 environment
Operator and patient must wear appropriate certified laser protective goggles for the used wavelength. Remove reflective objects, prevent unauthorized entry and keep the emergency stop accessible.
Perform and document the treatment
For point treatment hold the head steady; for scanning move at an even speed. Document the area, parameters, energy dose and patient response.
Frequently asked questions
6 W is the maximum nominal optical power. In maximum continuous operation this corresponds to up to 360 Joules per minute. In pulsed programs the average energy delivery may be lower.
The main advantage of higher power is faster dose delivery. Penetration is also determined by wavelength, tissue optical properties, spot size, contact and treatment geometry; 6 W alone does not mean three times the penetration depth.
Yes. The device is a Class 4 laser. Both operator and patient must wear certified laser protective goggles appropriate for the used wavelength.
Stop the device and seek urgent ophthalmological assessment. Provide the used wavelength and the possibility of exposure to a Class 4 laser up to 6 W. Absence of symptoms does not rule out injury.
Laser is not electrical stimulation, so a pacemaker does not automatically pose the same risk as electrotherapy. For implanted electronic devices, severe cardiac disease or chest treatments follow the manufacturer’s manual and treating physician's approval.
According to the source the package includes the 808 nm handpiece. 980 and 1064 nm handpieces are optional and are not considered part of the standard package.
The optical power is the same. The 6.0 is portable and smaller; the Pro is a desktop unit with a larger display designed for a fixed workstation.
There is no fixed number of sessions valid for all indications. Course length should be determined by diagnosis, tissue condition, dose, clinical response and rehabilitation plan.
What's included in the package?
- 1 pc PhysioLaser 6.0 Pro desktop central unit
- 1 pc 808 nm treatment head with 11 mm optics
- 1 pc operator laser protective goggles
- 1 pc patient laser protective goggles
- 1 pc power adapter
- 1 pc rechargeable battery
- 1 pc safety emergency stop
- 1 pc user manual
The goggles included in the package are intended for use with the standard 808 nm handpiece. For optional 980 or 1064 nm handpieces verify that the protective range and optical density of the goggles are appropriate for the given wavelength.
Protect the optical surface from scratches, dust and oily contamination. Clean only with materials and methods allowed in the user manual.
Do not use the device if the handpiece, cable, connector, goggles or optical surface is damaged.
Which professional PhysioLaser fits your clinic?
Technical specifications
| Laser type | GaAlAs diode laser |
| Standard wavelength | 808 nm with the handpiece included in the package |
| Optional wavelengths | According to the source 980 and 1064 nm handpieces may also be available; sold as accessories |
| Maximum optical power | 6 W, manufacturer tolerance: ±20% |
| Maximum theoretical energy delivery | 360 Joules per minute at maximum continuous power |
| Laser class | Class 4, CEI EN 60825-1 |
| Emission modes | Continuous and pulsed |
| Maximum frequency | 10,000 Hz |
| Base optics | 11 mm diameter, approximately 0.95 cm² treatment spot |
| Optional optics | According to the source a 22 mm, approximately 3.8 cm² optic may also be available |
| Programs | 85+ pre-set clinical protocols |
| Display | 3-inch backlit LCD |
| Power supply | Power adapter and rechargeable battery |
| Dimensions | 220 × 170 × 60 mm |
| Weight | Approximately 790 grams |
| Form factor | Desktop, suitable for placement on a treatment trolley |
| Regulatory classification | CE MDD, Class IIb medical device |
| SKU | G5764 |
| Manufacturer | Globus Italia, Italy |
When not to use the device?
- Never direct the laser beam at the eye or the immediate eye area.
- Do not apply over the abdomen or pelvic area during pregnancy.
- Do not apply directly over malignant tumours unless explicitly authorised by the treating physician.
- Do not apply over active bleeding or areas with significant bleeding tendency.
- For photosensitivity or photosensitising medication consult a physician first.
- Postpone treatment in febrile or acute systemic illness.
- Do not treat the thyroid and other endocrine glands directly.
- Investigate unknown swelling, pain or skin lesions before treatment.
For implanted electronic devices, severe cardiac disease or chest treatments follow the full manufacturer manual and medical approval. Detailed safety information →
Important information
The PhysioLaser 6.0 Pro is intended as an adjunctive treatment. It does not replace diagnosis, medical treatment, physiotherapy or appropriate rehabilitation.
Due to its Class 4 classification it must be used only by trained professionals in a proper laser safety environment. Higher power enables faster dose delivery but, with incorrect parameters, increases the risk of excessive dosing and tissue heating.
The product description is for informational purposes and does not constitute personalised medical advice or laser safety training. Cited studies are not device-specific evidence.
Scientific background
High-power laser therapy has been investigated in several musculoskeletal conditions. Studies used differing wavelengths, powers, doses and treatment protocols, so their results cannot be automatically generalised to all PhysioLaser programs.
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Ahmad MA et al. (2021):
Effects of low-level and high-intensity laser therapy as adjunctive to rehabilitation exercise on pain, stiffness and function in knee osteoarthritis: a systematic review and meta-analysis.
Physiotherapy.
PubMed
Systematic review in knee osteoarthritis. -
Abdildin Y et al. (2023):
High-intensity laser therapy in low back pain management: a systematic review with meta-analysis.
Lasers in Medical Science.
PubMed
Systematic review in low back pain. -
Barassi G et al. (2021):
Dual-wavelength high-power laser therapy and neuromuscular manual therapy in chronic neck pain: a randomized clinical trial.
Journal of Biological Regulators and Homeostatic Agents.
PubMed
Randomized trial in chronic neck pain with differing device protocols. -
Mostafa MSEM et al. (2022):
Effect of High-Power Laser Therapy Versus Shock Wave Therapy on Pain and Function in Knee Osteoarthritis Patients.
Photobiomodulation, Photomedicine, and Laser Surgery.
PubMed
Comparison of high-power laser and shock wave therapy in knee osteoarthritis. -
Verma S et al. (2022):
Effectiveness of High Power Laser Therapy on Pain and Isokinetic Peak Torque in Athletes with Proximal Hamstring Tendinopathy.
BioMed Research International.
PubMed
Study in athletes with proximal hamstring tendinopathy.
Looking for a desktop 6 W laser for fixed clinic use?
6 W power, 85+ protocols, 3-inch display and a desktop central unit suitable for placement on a treatment trolley.
Soft laser therapy – comprehensive guide →
PhysioLaser 6.0 – portable 6 W model →
PhysioLaser 12.0 – higher-power model →
Soft laser contraindications and safety information →