Medical Device Supply (Class II)

The contract involves the supply of FDA-regulated Class II medical devices that must have obtained 510(k) clearance and be manufactured in compliance with current good manufacturing practices and applicable quality standards. All products must meet stringent regulatory and performance requirements to ensure safety and efficacy for use in medical settings. The solicitation is structured as a subcontract under the Department of Defense’s Medical Supply Chain initiative, with performance required at Joint Base Andrews, Maryland 20762. The opportunity was posted on July 26, 2026, and responses are due by August 3, 2026. The North American Industry Classification System code 339112 applies, indicating the focus on surgical and medical instrument manufacturing. While no set-aside designation is specified, the procurement is part of a broader federal effort to secure reliable sourcing of critical medical equipment for military and healthcare operations.