State-of-Art Facility

Our state-of-the-art manufacturing facility is powered by world-class equipment, enabling efficient and controlled production processes. Manufacturing is carried out in an ISO-compliant cleanroom to ensure the highest standards of quality, precision, and safety.

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EN ISO 13485:2016 Certified

Being EN ISO 13485:2016 certified, we adhere to stringent international quality management standards for medical devices. This certification reinforces our commitment to excellence, risk management, and patient safety across all stages of manufacturing..

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CDSCO Approved

All our products are CDSCO approved, meeting the regulatory requirements set by the Central Drugs Standard Control Organization (CDSCO), Government of India, to ensure safety, quality, and performance.

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A Complete
Regenerative Medical Devices
Under One Roof

PRP KIT, GFC KIT, PRF KIT, FAT GRAFTING KIT, SVF KIT, EXOSOMES

About Sishya Meditech
Our Vision

To become a trusted and globally recognized medical device manufacturer by delivering innovative solutions, maintaining uncompromised quality, and contributing to improved patient outcomes across healthcare markets.

Our Mission

To design and manufacture high-quality, safe, and reliable medical devices by adhering to international quality standards, regulatory requirements, and ethical business practices, while continuously improving our processes to meet the evolving needs of healthcare professionals and patients.

Our Values
  • Quality First – We prioritize product quality, safety, and compliance in everything we do.
  • Customer Commitment – We focus on understanding and fulfilling the needs of healthcare professionals and partners.
  • Continuous Improvement – We embrace innovation, learning, and process excellence.
  • Regulatory Compliance – We strictly adhere to national and international regulatory standards.

Who We Are?

We are a quality-driven medical device manufacturing company committed to delivering safe, reliable, and innovative healthcare solutions. With a strong focus on Clinical Efficacy, Regulatory Compliance, Precision Manufacturing, and Continuous Improvement, we design and manufacture medical devices that meet both national and international standards.

Our state-of-the-art facility operates within an ISO-standard cleanroom environment and follows a robust quality management system certified to ISO 13485:2016. All our products are developed and manufactured in compliance with the Medical Devices Rules, 2017, and are approved by CDSCO, Government of India.

Backed by a skilled team of professionals and modern manufacturing infrastructure, we work closely with healthcare professionals, distributors, and partners to deliver consistent quality, reliability, and value—contributing to improved patient outcomes and advancing healthcare excellence.