Meet SCENAR
SCENAR™ is an FDA-cleared, handheld medical device designed for rapid, non-invasive pain relief and functional restoration.
Developed for clinical use, SCENAR utilizes adaptive electrical impulses and real-time biofeedback to stimulate the body’s own regulatory and healing mechanisms.
Key benefits
Rapid pain relief
Clinically proven to reduce acute and chronic pain by activating endogenous neuropeptide pathways.
Non-invasive & drug-free
Delivers gentle, safe therapy with no known side effects—suitable for adults, children, and sensitive patient groups.
Adaptive, personalized treatment
Real-time biofeedback ensures each impulse is tailored to the patient’s physiological response for optimized outcomes.
Broad clinical utility
Effective for a wide range of musculoskeletal, neurological, inflammatory, and stress-related conditions.
How it works
Scenar is a handheld, non-invasive device that delivers adaptive electrical impulses directly to the skin. These impulses closely mimic the body’s own nerve signals, enabling direct communication with the nervous system and stimulating the release of neuropeptides—key regulators of pain and healing
- Biofeedback-Driven: SCENAR continuously monitors changes in skin impedance and adjusts its impulses in real time, ensuring each treatment is individualized and optimized for the patient’s physiological response.
- C-Fiber Stimulation: The device targets small unmyelinated C-fibers, which make up the majority of peripheral nerves and are responsible for neuropeptide production. This stimulation catalyzes the body’s internal pain modulation and healing processes.
- Reflex Biofeedback: Unlike traditional electrotherapy, SCENAR engages in a two-way “conversation” with the body, interpreting neural feedback and adapting every signal for maximum therapeutic effect.
- Sustained Effect: The neuropeptides released during treatment continue to support healing for several hours after a session, contributing to lasting pain relief and functional improvemen
Technical and Regulatory
FDA Cleared
SCENAR™ devices are FDA-cleared for the treatment and management of acute and chronic pain, including post-surgical and post-traumatic pain.
CE Marked & ISO Certified
SCENAR holds CE certification for pain relief in the EU and meets ISO 9001 and ISO 13485 international quality management standards for medical devices.
Device Specifications
- Power Supply: 4 x AAA batteries
- Frequency Range: 15 Hz – 350 Hz
- Amplitude & Frequency Modulation: Multiple preset and customizable modes
- Display: LCD (varies by model)
- Weight: ~0.4 kg; Dimensions: 190 x 70 x 40 mm
Safety
SCENAR is non-invasive, with no known side effects. It is contraindicated only for patients with cardiac pacemakers or certain neurological conditions.
Warranty
Devices include a two-year limited warranty from the manufacturer.
Global Compliance
SCENAR is registered and approved for medical use in over 36 countries, including the US, EU, Israel, Australia, and more.