Nitrogen cooling cryotherapy cabin CRYO XC™

Overview
The CRYO XC™ whole-body cryotherapy chamber is a non-medical LN2-based unit engineered for short-duration extreme-cold exposure. Recommended session temperatures typically range from -110°C to -140°C (-170°F to -200°F), with defined expanded limits under specified conditions. The system produces cool vapors forming a vortex of cold air around the user to deliver a dry, evenly distributed thermal stimulus in brief treatment intervals.

Intended users

• Professional and amateur athletes and sports organisations
• Recovery and wellness centres, spas and beauty clinics
• Physiotherapists, rehabilitation facilities and select medical/clinical settings
• Private/home wellness users (selected non-pressurized configurations)

Systems (storage & supply options)

• Pressurized system — uses pressurized LN2 tanks/vessels; recommended for high-throughput locations and facilities with on-site LN2 logistics.
• Non-pressurized system — uses non-pressurized dewars (typically 2 × 50 L included); suited to smaller centres, spas, startups and private installations where flexibility is required.

Safety & operational features

• Forced/exhaust ventilation and vapor deflectors for controlled vapor handling
• Active drying mode and cabin lift/door sensors (in higher configurations)
• Session tracking/logging, remote diagnostics and service support
• Emergency stop and multiple cabin-monitoring options on Plus configurations

Customization & installation
Exterior and interior finish options, brand customization and left/right installation orientation are available. Some models allow a dual-door cabin. Installation requires a room with active ventilation/AC and a reliable LN2 supply; typical recommended room footprint and constraints are provided in technical documentation.

Specifications

• Model: CRYO XC™ (whole-body cryotherapy chamber)
• Session temperature (recommended): -110°C to -140°C (-170°F to -200°F)
• Session temperature (maximum/expanded): down to -160°C (-240°F) under specified conditions
• LN2 consumption (typical): Pressurized: 5–8 L/session; Non-pressurized: 4–7 L/session
• Storage tanks: Pressurized tanks (not included) or non-pressurized dewars (2 × 50 L included with non-pressurized system)
• Electrical: 230 V, 50 Hz (60 Hz compatible), min. 16 A, max power 4000 W
• Certification/classification: CE marked; evaluated by FDA under 513(g) — classified as non-medical device
• Installation footprint: recommended min. ~12 m², optimal ~20–25 m² depending on layout
• Physical dimensions (approx.): 2200 × 950 × 1500 mm; weight ≈ 370 kg

Typical use cases

• Cryotherapy and recovery centres seeking high throughput treatments
• Sports teams and athlete performance/recovery protocols
• Rehabilitation clinics and physiotherapy practices as an adjunct modality
• Selected private/home wellness setups using non-pressurized models

Documentation & support
Comprehensive product literature (brochure and technical specs) is available as downloadable resources. Remote diagnostics, maintenance guidance and service support are provided to facilitate operation and uptime.