VERTEX
Passive cervical exoskeleton prototype available for paid pilot testing on request; not a medical device.
Product Overview
VERTEX is a passive cervical exoskeleton prototype from Zeta Industries that uses interchangeable elastic resistance for neck-muscle training. The current experimental device is intended for physical-exercise activities and technical evaluation; it is not a medical device and is neither intended nor authorized for therapeutic or rehabilitative use. Paid pilot testing is available on request with customized case-by-case pricing; Zeta forecasts general launch in 2027, with a planned €400 reference consumer price rather than a current retail price.
Positioning & Buyer Fit
Passive cervical exoskeleton prototype available for paid pilot testing and technical evaluation; non-medical.
Organisations and researchers evaluating an experimental, non-medical cervical-training system in controlled physical-exercise or technical-evaluation contexts.
Use Case & Product Classification
Head and neck support exoskeleton
Product Highlights & Manufacturer Claims
- Passive elastic-resistance system
- 800 g (±5%)
- five interchangeable elastic options with indicative 10–150 N force per elastic at typical working elongation
- S/M and L/XL sizes
- 400–590 mm size-dependent dimension
- carbon-fiber rods
- PLA frame with 10% additive
- foam/polyester/elastane braces and cap
- latex-rubber elastics
- full natural neck movement design.
Paid pilot testing is available on request, with customized case-by-case pricing. General launch is forecast for 2027; the planned €400 consumer reference price is not a current retail price. The consumer app is planned as freemium for one user; business use is planned as a monthly organisational subscription for organisations with multiple profiles. No CE marking, MDR status, certification, or therapeutic or rehabilitative authorization has been recorded.
Official datasheet notice governs the representation: experimental prototype for cervical-muscle training only; non-medical and not authorized for therapeutic or rehabilitative use.
Certification & Regulatory Notes
Not a medical device under Regulation (EU) 2017/745; not intended or authorized for therapeutic or rehabilitative use.
Pricing & Commercial Access
Contact manufacturer for current pricing
Quote-Based
Quote Based
Not specified
Unknown
09/09/2026
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