01
Accreditation and the MDIA Badge
A rigorous, audited standard for industry best practices, device authentication, storage, and regulatory compliance. The MDIA badge is intended to give buyers a clear verification path once accreditation launches.
Formation Phase
Setting the standard for integrity in the medical device secondary market.
The Medical Device Integrity Alliance is establishing an accreditation standard, verifiable badge, and unified voice for the independent secondary market for new medical devices.
About MDIA
An institutional standard for a market built on trust.
The Medical Device Integrity Alliance is a formation-stage trade association for qualified independent companies serving the secondary market for new medical devices.
MDIA exists to make integrity visible, auditable, and easier for buyers to evaluate. The organization is developing accreditation, badge verification, vendor vetting, and policy advocacy for a market that has historically lacked a unified institutional standard.
MDIA does not publish member lists, governance rosters, dues, or registry records until those materials are formally approved for public release.
Mission
A standard buyers can trust.
The independent secondary market for new medical devices serves hospitals, surgery centers, and clinics with legitimately sourced capital equipment and disposables. It has historically lacked a unified standard, an accreditation body, and a coordinated voice in policy.
MDIA exists to change that. We accredit independent companies against a rigorous standard for industry best practices, device authentication, storage, and regulatory compliance. We issue a verifiable badge that hospitals and procurement teams can trust. We provide vendor vetting and shared services that strengthen our members' operations. And we advocate for the legal, regulatory, and policy positions that allow legitimate secondary commerce in medical devices to thrive.
Our standard is the floor, not the ceiling. Membership is open to any company that meets it.
What We Do
Core functions for a credible market.
02
Vendor Vetting and Shared Services
Background checks, financial verification, and accreditation of logistics, authentication, and sterilization vendors. Vetted once, trusted across the membership.
03
Policy and Advocacy
A unified industry voice on legal, regulatory, and policy questions affecting the secondary market for medical devices, including device resale rights, FDA clarity, and supply chain transparency.
04
Industry Standards and Intelligence
Briefings on regulatory changes, channel actions, and procurement trends. Member-developed and member-governed standards that evolve with the industry.
For Buyers
Verification at launch.
Hospitals, group purchasing organizations, and clinical buyers will be able to verify companies displaying the MDIA badge through a public registry once the accreditation program launches. Accredited members are audited against a documented standard for industry best practices, authenticity, storage, and regulatory compliance.
Membership
Open to qualified independent companies.
Membership in MDIA is intended for qualified companies in the independent secondary market for new medical devices that successfully complete accreditation against the MDIA Standard. We are currently in formation phase and accepting member inquiries from companies preparing for accreditation.
Contact
Get in touch.
Prospective members, buyers, press, and policy contacts can reach us directly.