Certifications
FDA Registration
LINEMASTER SWITCH CORPORATION is FDA Registered since 2006. Our registration number is 3001592626.
LINEMASTER registration page on the FDA
ISO 13485 Certification
ISO 13485 is the internationally recognized Quality Management Systems Standard that is established for the design and manufacture of medical devices. Linemaster has demonstrated the ability to successfully implement a comprehensive management system for the design and manufacture of medical devices that meets the ISO 13485 Standard, FDA QSR, and regulatory requirements.
Pharmaceuticals and Medical Devices Agency, Japan
Pharmaceuticals and Medical Devices Agency, Japan
Request Custom Footswitches
Linemaster’s custom footswitches are designed to meet specific user requirements, offering a range of features such as various pedal configurations, wired and wireless options, and customizable LED indicators. These custom foot controls provide reliable, durable solutions tailored to enhance functionality in diverse applications.
Our Learning Center
The Linemaster Learning Center offers resources to help customers understand and effectively use their medical and industrial foot controls. This educational hub provides valuable insights into product features, applications, and maintenance, ensuring users maximize the benefits of their Linemaster solutions.