Rayboen has officially passed the annual audit of the ISO9001 Quality Management System, confirming that the company’s quality management, standardized processes and service management fully comply with international quality standards. The annual review covered the full business process, including order management, R&D, production, quality inspection and after-sales service. With strict assessment on quality control, risk management, customer response and continuous improvement, the audit fully recognized Rayboen’s stable and reliable management capabilities. As a globally recognized quality benchmark, ISO9001 underpins Rayboen’s consistent high-standard quality philosophy. This successful annual review ensures standardized, controllable and traceable operations, guaranteeing stable product quality and reliable delivery. Moving forward, Rayboen will continue to optimize its management system, upgrade refined and scientific management, and always provide customers with trustworthy products and professional services.

April 21, 2026 — Rayboen successfully held the kick-off meeting for the ISO 13485:2016 Medical Device Quality Management System Certification Project. Attended by the company’s senior management team, department leaders and key core employees, the meeting marks a pivotal step forward for Rayboen in medical compliance, quality control and global development strategy. Key Highlights of the Meeting The meeting officially announced the full implementation of the ISO 13485:2016 international standard, aiming to establish a professional medical device quality management system that covers the entire process: design and development, procurement and supply, production and manufacturing, quality control, packaging and delivery, as well as after-sales service. The meeting clarified project goals, implementation plans, role division and schedule milestones. It emphasized taking risk management as the core, regulatory compliance as the bottom line, and quality as the top priority, integrating system requirements into daily operations in depth to ensure product safety, efficacy and traceability. The launch of this certification not only realizes a systematic upgrade of the existing quality management system, but also serves as a strategic layout for the company to deepen its footprint in the medical industry and expand global business. About ISO 13485:2016 ISO 13485:2016 is a dedicated quality management system standard for the medical device industry issued by the International Organization for Standardization (ISO). It focuses on regulatory compliance, risk management and full life cycle quality control, and is widely applicable to enterprises engaged in the design, production and service of medical devices, supporting components and consumables. This standard has become the core market access requirement and credibility benchmark for global regulatory authorities including EU MDR, US FDA QSR and China NMPA, as well as international customers worldwide. The initiation of ISO 13485:2016 certification is an important milestone in the company’s development. In the future, Rayboen will take the system establishment as an opportunity to continuously optimize processes, strictly control product quality and strengthen compliance management. The company strives to obtain the certification as soon as possible, repay customers with higher-standard products and services, and contribute to the development of the global healthcare industry.

On April 16, 2026，our company recently had the pleasure of welcoming a distinguished customer from Chile to our manufacturing facility for technical communication and on-site inspection. The visit aimed to discuss customized product development, mold design, injection molding processes, quality control, and long-term supply cooperation. Leo Zhang, the founder of our company, held in-depth discussions with the customer about the intended product, including product structure, material selection, mold development cycle, production efficiency, and quality assurance standards. Both sides reached a clear consensus on project positioning and technical requirements. Accompanied by Leo Zhang, the customer fully inspected our production lines, including EDM machining, precision mold workshop, quality testing, ultrasonic welding and air-tightness inspection, class 100,000 clean injection molding workshop, product assembly, and packaging workshop. The customer highly praised our advanced equipment, strict quality management system, clean production environment, and integrated one-stop manufacturing capacity from mold to finished product. This visit further strengthened mutual trust and laid a solid foundation for in-depth cooperation. We will continue to provide reliable, high-precision, and efficient mold manufacturing and injection molding services for global customers.

On November 10, 2025, the Aikem team and the Rayboen team conducted detailed planning and communication regarding medical product processing orders. Mr. Zhang, the company’s Project General Manager, personally led the Quality Manager and Business Manager to accompany the client throughout the process, providing the most professional services and guidance. The Aikem team spoke highly of Rayboen’s production equipment and process flow. This exchange is not only a cooperation negotiation, but also an opportunity to achieve complementary advantages and coordinated development at the industrial chain level. We will join hands to explore the future development of the medical industry and realize win-win cooperation! The arrival of the Aikem team at our factory kicked off a splendid exchange tour! The team first visited the Testing Department to inspect our advanced automated testing equipment on site, including engineering design and 3D testing auxiliary equipment, and gained a comprehensive and in-depth understanding of every detail and precision. Subsequently, the team visited the EDM Processing Workshop and the Mold Assembly Workshop one after another to experience the unique charm of mechanical operation firsthand. They also visited the Design Department and Quality Inspection Room to explore the exquisite craftsmanship behind each product. Finally, the Aikem team walked into the Medical Injection Molding Workshop, conducted in-depth exchanges and interactions with our side, and put forward many valuable feedback and suggestions. This visit not only allowed the distinguished guests to intuitively feel our factory’s efficient operation mode and professional management system, but also demonstrated the Aikem team’s ultimate pursuit of quality, technology and innovation. This exchange tour is not only a visual feast, but also a knowledge feast of ideological collisions and inspired inspiration!

On January 13, 2026, Rayboen was approved as a Specialized, Sophisticated, Unique and New Small and Medium-sized Enterprise. Recently, Shenzhen Rayboen Plastic MoldCo., Ltd. has been awarded the title of Specialized, Sophisticated, Unique and New Small and Medium-sized Enterprise, which fully demonstrates the company’s strong strength in technological innovation and professional manufacturing. The company specializes in product development and structural design, mold scheme design and processing, molding technologies including injection molding and ultrasonic welding, as well as product assembly. It has a professional technical team with more than 15 years of industry experience, and is equipped with advanced production and testing equipment such as CNC precision machine tools and all-electric high-speed injection molding machines. Adhering strictly to cleanliness and safety standards, the company is committed to becoming a reliable and trusted provider of integrated plastic mold solutions in the industry.