Skaphor — FDA CE approved eye therapy device for advanced eye care

Skaphor — FDA CE approved eye therapy device for advanced eye care

Trusted Medical-Grade Innovation

Founded in 2018, Guangzhou Ruiheng Electronic Technology Co., Ltd. (brand: Skaphor) is a national high-tech enterprise integrating R&D, production and sales. With the mission of scientific eye care, guarding eyesight, we develop medical-grade solutions including the FDA CE approved eye therapy device line. Our products combine rigorous clinical validation and industrialized innovation to ensure safe, effective eye health management.

Clinically Effective Solutions

Skaphor devices address common ocular conditions — dry eye, meibomian gland dysfunction and fatigue-related eye strain — using evidence-based modalities. Each unit delivers precise, controllable therapy that clinicians and users trust. Our medical-grade systems are designed to support long-term eye health and integrate into clinical protocols as well as at-home care plans.

Intelligent Design & User Experience

Ergonomics, ease-of-use and intelligent controls define Skaphor products. From intuitive touch panels to compact, portable models, our eye therapy devices are engineered for clinician efficiency and patient comfort. Smart treatment presets, safety lockouts and clear guidance make therapeutic sessions reproducible and user-friendly across age groups.

Quality, Compliance and Global Reach

As a manufacturer committed to excellence, Skaphor maintains strict quality control and regulatory compliance. Our FDA CE approved eye therapy device portfolio meets international standards and is distributed across 30+ countries and regions including Europe, the United States, Asia-Pacific and the Middle East. We combine medical oversight with scalable manufacturing to ensure product reliability.

Why Choose Skaphor

Choose Skaphor for clinically proven technology, medical-grade safety and global support. Whether equipping a clinic or implementing a home-care program, our products improve outcomes and user satisfaction. Learn more at https://www.skaphor.net/ and contact our team for product demos, clinical data and distribution partnerships.

FDA CE approved eye therapy device Display

FAQ:
What is the source of clinical data?

6-month double-blind trial report issued by the partner tertiary hospital (can be provided after signing the NDA).

Is there any exclusive logistics program for large orders?

More than 500 units, we can provide dedicated logistics (including export customs clearance/destination country customs clearance).

Can I be authorized to use medical endorsement?

Signed distributors can use the “Zhongshan Ophthalmic Center Technical Cooperation Unit” logo (subject to audit).

Do you provide sales kits?

Provide kits containing qualification documents, clinical data, product promotional materials, clinical cases, etc.

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