FDA-Compliant Medical Device Manufacturing

The contract requires the manufacture of clinical distant vision acuity testing chart sets that meet FDA regulations, DLA technical specifications, and ASTM D3951 packaging standards, ensuring medical device compliance and safe handling for clinical use. The equipment must be produced to precise technical criteria to maintain accuracy and consistency in vision testing environments. All units must be packaged in accordance with ASTM D3951 to protect against damage during storage and transit, and the final product must satisfy the stringent quality controls mandated by the FDA and the Department of Defense. This is a subcontract opportunity posted on July 30, 2026, with a response deadline of August 5, 2026. The North American Industry Classification System code is 339112, indicating the focus is on medical and dental equipment manufacturing. The place of performance is listed as FPO with ZIP code 96675, and the contracting agency is the Department of Defense under the Medical Supply Chain MD Surg FSF. Although no point of contact information is provided, interested parties must submit proposals through the official DIBBS portal via the provided UI link to participate in the solicitation.