Ophthalmic Lens Manufacturing (Class III Medical Device)

The contract pertains to the manufacture of FDA-regulated Class III ophthalmic lenses, which are high-risk medical devices requiring strict adherence to Good Manufacturing Practices and comprehensive traceability throughout production and distribution. Compliance with stringent labeling requirements and Department of Defense Defense Logistics Agency technical standards is mandatory to ensure product safety, efficacy, and regulatory approval. The work must be performed at Fort Hood, Texas, with all manufacturing and quality control processes aligned to federal medical device regulations and defense supply chain protocols. The solicitation is structured as a subcontract opportunity with a narrow response window closing on July 21, 2026, and is governed under NAICS code 339113 for medical equipment and supplies manufacturing. All parties must demonstrate proven capability in producing Class III devices under GMP frameworks and be prepared for rigorous inspection and documentation audits.