Surgical Technology Laboratories/DBA Surgiform is a FDA registered medical device establishment (Establishment # 1825527) operating in compliance with 21 CFR 820 (current Good Manufacturing Practices) and ISO13485:2016 (Medical Device - Quality Management Systems).
Quality Policy -
STL/Surgiform is committed to providing high quality, safe medical products and to maintaining the effectiveness and compliance of our Quality Management System.
- We will manufacture products in compliance with our established procedures.
- We will strive to meet or exceed our customers’ expectations.
- We will seek continuous improvement and will maintain a business environment in which quality and customer satisfaction are the organization’s highest priorities.
- We operate in accordance with current 21 CFR Part 820 Quality System Regulations and compliance with ISO 13485:2016.
Links to Registrations and Certifications –
Surgiform ISO Certification
