FDA-Regulated Medical Device Component Supply

This subcontract involves the manufacture of medical device components for prime contractors supporting Defense Logistics Agency supply contracts. The selected provider must produce parts in strict accordance with the DLA Master List of Technical and Quality Requirements, specifically adhering to R and I numbers. All production must utilize traditional manufacturing processes, as additive manufacturing is explicitly prohibited, and the provider must possess equipment capable of meeting FDA-regulated medical grade standards. Managed by the Department of Defense under the Medical Supply Chain MD Surg FSF, the contract is categorized under NAICS code 339112. Performance for the delivery of finished components will take place in San Antonio, Texas. Interested parties should note the response deadline of September 8, 2026.