Design Intelligence

Our industrial design team bridges aesthetic vision with optical engineering, guiding projects from initial sketch through mass production. The development pipeline moves through four distinct phases—concept sketching, 3D modeling, functional prototyping, and final production—delivering market-ready products in as little as 30 days from concept approval. Our portfolio spans 200+ developed SKUs across four core form factors: panel systems, facial masks, wearable caps, and flexible wraps. Each platform can be adapted to existing specifications or fully reimagined through proprietary mold development, allowing partner brands to launch distinctive product lines without investing in internal R&D infrastructure. We maintain active OEM and ODM partnerships with over 50 global brands, with client identities protected under strict confidentiality agreements. Whether refining an established product architecture or engineering entirely new device categories, we translate brand identity into tangible product experiences that meet both optical performance targets and manufacturing scalability requirements.

Manufacturing Precision

Our 10,000㎡ vertically integrated facility in Shenzhen houses end-to-end production lines spanning SMT, precision molding, and final assembly. With 200 staff including 35 optical engineers, we maintain complete control over critical processes—from 95% self-developed mold tooling to high-speed component placement at ±0.05mm precision. Surface-mount technology operates at 50,000 components per hour, ensuring consistent optical alignment across high-density LED matrices, while proprietary thermal management combines directional airflow engineering with anodized aluminum heat sinks for stable extended operation. Core technical barriers include medical-grade wavelength calibration (850nm/660nm dual-band at ±5nm tolerance) and multi-spectrum synergy optimization, supported by 150+ optical patents and ISO 13485/EU MDR compliance. Each unit undergoes 100% four-hour burn-in testing with integrating sphere verification before shipment. This process discipline delivers 10,000 units daily output while maintaining identical specifications whether your order is a single prototype or a full container load.

Global Market Access for Red Light Therapy

Every red light therapy device we manufacture ships with complete regulatory documentation, enabling immediate market entry across North America, Europe, and Asia-Pacific. Our quality management system is built on ISO 13485 medical device standards—applied to every product tier from consumer wellness panels to professional-grade installations.

Certification coverage includes:

FDA 510(k) Exempt classification for general wellness distribution in the United States

CE Marking (MDR Class I) with full EU technical documentation

EMC & Safety compliance (FCC Part 15, EN 60601-1-2, EN 62368-1)

Material safety (RoHS 3.0, REACH SVHC screening)

Quality assurance at volume:

100% burn-in testing (4-hour continuous operation), ±5nm wavelength binning, and lot-traceable component sourcing. Whether your order is 100 units or 10,000, every red light therapy system meets the same optical and safety specifications—backed by Certificate of Conformity and test reports for customs clearance.