CONSOLIDATED MACHINE CORP

Consolidated Machine Corp specializes in the precision manufacturing of specialized surgical appliances and medical equipment, with demonstrated expertise in designing and producing autoclaves featuring integrated electric steam generation systems. Their technical capabilities center on high-precision metal fabrication, thermal system integration, and medical-grade sterilization technology compliant with healthcare industry standards. The company’s engineering focus includes automated control systems, pressure vessel design, and electro-mechanical assembly tailored for sterile processing environments in clinical and laboratory settings. Their ability to deliver fully integrated steam generation solutions suggests deep competency in thermal dynamics, electrical safety protocols, and FDA-regulated manufacturing processes, positioning them as a niche supplier of mission-critical sterilization equipment. The contractor has delivered products to the U.S. Department of Agriculture, indicating experience supporting federal research, veterinary, or food safety facilities that require reliable, high-performance sterilization systems. This relationship suggests alignment with agency needs for biocontainment, equipment decontamination, and laboratory hygiene infrastructure—areas where precision and regulatory adherence are paramount. Their primary industry focus is on NAICS 339113, which encompasses the manufacturing of surgical appliances and supplies, particularly devices requiring sterile processing capabilities. This vertical specialization places them within the medical device supply chain, serving institutions that demand validated, repeatable sterilization performance. Their market positioning is that of a technical manufacturer serving regulated healthcare and scientific environments rather than mass-market medical product distributors. Consolidated Machine Corp is a small business structured as a 2L entity, headquartered in Billerica, Massachusetts. While no government certifications are currently listed, their production capabilities reflect adherence to quality systems typical of medical device manufacturing, including potential compliance with ISO 13485 and cGMP standards. Their geographic presence in New England supports proximity to biomedical research hubs and federal facilities requiring domestic, reliable manufacturing partners.