Rehabilitation Technology.
Precisely Developed.

Therapeutic systems developed to meet defined medical device standards and operational requirements.
URSA™
TECAR RC-448K
CE Medical Device Compliance

URSA™ REHABILITATION SYSTEMS

URSA systems are engineered around core therapeutic mechanisms rather than bundled feature sets. Each modality represents an independent, purpose-built control architecture optimized for its energy delivery method.

ELECTRO Therapy
SYSTEMS

Multi-channel electrotherapy systems designed for structured treatment protocols.

SHOCKWAVE THERAPY
SYSTEMS

Focused and radial shockwave systems for musculoskeletal treatment

TECAR Therapy
SYSTEMS

Capacitive and resistive radiofrequency systems for therapeutic application.

Additional Rehabilitation Systems

Including ultrasound therapy, traction systems, and integrated rehabilitation units.

ULTRASOUND Therapy
SYSTEMS

Precision ultrasound systems developed for targeted tissue stimulation and rehabilitation support.

An Engineered Approach To Rehabilitation Technology.

URSA develops rehabilitation systems through a focused, application-driven process.
Each platform is designed around a specific therapeutic purpose—selected, configured, and refined to meet defined rehabilitation needs.
Rather than maximizing features or modalities, URSA prioritizes control, safety, and operational clarity—ensuring every system performs exactly as intended in professional practice.

Compliance Is Baseline

Regulatory compliance is treated as a starting point, not a differentiator.

Defined Operating Logic

URSA systems are engineered for consistent, repeatable operation across users and environments.

Long-Term Platform Stability

Core platforms remain stable across product cycles to protect training and investment.

Short Learning Curve

URSA systems are engineered to require minimal training without sacrificing control.

Quality & Compliance

URSA systems are developed with a focus on controlled energy delivery, electrical safety, and long-term operational stability.
Design decisions prioritize repeatability, serviceability, and predictable behavior under clinical operating conditions. Compliance is treated as a baseline requirement, not a differentiator, and is integrated throughout the development and validation process.
Technical documentation, system specifications, and compliance-related materials are maintained as part of the product lifecycle and are available upon request to qualified partners.

Distribution & Support

URSA systems are supplied exclusively through authorized distribution partners. This model ensures controlled deployment, localized support, and alignment with professional clinical requirements.
Technical support, service procedures, and system maintenance are structured to support long-term operation across distributed clinical environments. Support materials and service documentation are provided through authorized channels.

Contact URSA

URSA systems are supplied through authorized distribution partners.
Submit an inquiry to receive technical documentation and local availability details.
Technical specifications and system documentation
Localized Support and availability
Distribution partnership inquiries for qualified regional partners