Treat tinnitus in 20 minutes a day without risk.
Relief from the first few weeks
CE certified medical device
10,000+ Devices Sold
Try it without obligation, pay in 3 installments
How MedTool One Works
MedTool One uses low-intensity laser technology (650 nm, 5 mW) designed to precisely target the cochlea. The laser light stimulates the mitochondria (the "power plants" of cells), promoting the production of ATP , the essential "fuel" for cell regeneration. This process, known as photobiostimulation, activates microcirculation, accelerates cell proliferation, and supports the repair of damaged tissue in the auditory system. The result? Concrete and innovative support for restoring inner ear function. This one-of-a-kind technology was developed to offer an advanced, non-invasive solution for tinnitus treatment.
Stimulates mitochondria
Activates the microcirculation
Restore functionality
Benefits for your well-being
Thanks to its synergistic action, MedTool One promotes an environment conducive to the natural recovery of the inner ear, with tangible results after just the first 12 weeks.
Reduction of whistling and buzzing
Improved sleep
Restoring functionality
0k+
Devices sold in Europe
0 out of 10
Satisfied customers after the cycle
0min
Daily treatment
0 years
Of studies and active research
RECENSIONI
Testimonianze di chi ci ha provati
They say about us

"My son Andrea, who suffers from bilateral tinnitus, began therapy. After just 30 days, he noticed a marked improvement ."

Stefania Moretti

Try it without obligation
1 — Activate the trial with €149
Relief noticeable from the first few weeks

2 — Use the device for 90 days

During the trial, 2 installments of €99 for use.

3 — Before the 90th day choose whether to:

  • Keep it forever – €630
  • Continue in installments – €99/month for 6 months
  • Return it for FREE

✓ No hidden costs

✓ You decide how to proceed

Research and science at our side

In collaboration with San Raffaele Hospital and Piacenza Hospital

Med Tools Solutions works closely with universities, research centers, and medical-scientific specialists to develop increasingly effective and safe devices.

Thanks to these collaborations we can:
  • Validate our products with clinical studies and scientific protocols
  • Integrating the latest discoveries in the field of laser photobiostimulation
  • Ensure high standards of quality and reliability

Constant dialogue with doctors and researchers allows us to transform research into concrete solutions, improving the lives of those suffering from tinnitus and hearing disorders.

FAQ

How long does it take to notice an improvement?
Does it work even if I've had tinnitus for years?
Does the device completely eliminate tinnitus?
Can I use it if I wear hearing aids or have other hearing problems?
Is it difficult to use?
How many times a day should it be used?
Are there any side effects?
What does the trial include?
What happens after 90 days?
The benefits you will get
Real benefits for your hearing health
MedTool One® is more than just a device: it's a daily ally in managing tinnitus. Thanks to low-intensity laser photobiostimulation (650 nm, 5 mW), it creates an environment conducive to the natural recovery of the inner ear, with tangible results after just the first few weeks.
Certified device
EC 93/42/EEC

The CE marking indicates a product's conformity to Community requirements regarding safety, health and environmental protection, for which the manufacturer is responsible.

EN 60601-1-2
The EN 60601-1-2 standard defines the requirements and tests to ensure the safety and electromagnetic compatibility of medical electrical equipment.
UNI EN ISO 14971

The UNI EN ISO 14971 standard establishes the criteria for risk management applied to medical devices throughout the entire product life cycle.

EN 60825-1
The EN 60825-1 standard defines the safety requirements and classification of laser products for eye and skin protection.
CE 93/42/CEE

La marcatura CE indica la conformità di un prodotto ai requisiti comunitari in materia di sicurezza, salute e protezione dell’ambiente, di cui è responsabile il produttore dello stesso.

EN 60825-1
La norma EN 60601-1-2 definisce i requisiti e le prove per garantire la sicurezza e la compatibilità elettromagnetica delle apparecchiature elettromedicali.
UNI EN ISO 14971

La norma UNI EN ISO 14971 stabilisce i criteri per la gestione dei rischi applicata ai dispositivi medici durante l’intero ciclo di vita del prodotto.