Certifications & Compliance
When you're purchasing equipment for clinical use, documentation matters. All Parico products go through rigorous testing and third-party certification before reaching our warehouse. Below is an overview of our certifications and what they mean for your clinic.
FDA — US Food & Drug Administration
Clearance from the US federal agency responsible for regulating medical devices. Confirms products meet US safety and performance requirements.
ISO 13485 — Quality Management System
International standard for medical device quality management systems. Ensures consistent design, development, production, and post-market surveillance processes.
CE — European Conformity
While required for European markets, our CE mark demonstrates to our US clients our commitment to passing the world's most rigorous safety and environmental standards
