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 Foot Switches
Linemaster designs custom foot switches to fit the specific needs of each application. Options can include different pedal configurations, wired or wireless designs, and customizable LED indicators, depending on what the user and the equipment require. The goal is not just to offer more choices, but to deliver a foot control that feels purposeful, reliable, and built to perform in real-world environments where durability and consistency matter.
Our Learning Center
The Linemaster Learning Center is a hub for answers and practical guidance about medical and industrial foot switches. It brings together FAQs, product insights, and application-focused resources to help customers better understand their options and make confident, informed decisions.