MedTech

Medical device companies rely on SKP Med-Tech for exceptional manufacturing solutions that consistently deliver high-quality, mission-critical products. With our FDA 510(k)* and ISO 13485** certification, we not only meet but exceed the rigorous standards of the medical device industry in the United States and globally, solidifying our position as a leader in quality and reliability.

Whether you are an innovative startup or a powerful global healthcare entity, we forge enduring partnerships by providing unparalleled manufacturing and supply chain solutions. Our unwavering commitment to quality, strict adherence to regulatory requirements, and a distinguished legacy of technological excellence set us apart.

Choose SKP Med-Tech to elevate your product manufacturing and secure your success in the fiercely competitive healthcare landscape.

*The FDA 510(k) certification is required by the U.S. Food and Drug Administration (FDA) for companies that want to market medical devices in the United States.
**International standard for quality management systems (QMS) specifically for the medical device industry