Ms. Megan Riccobuono

Ms. Megan Riccobuono serves as a Clinical Analyst responsible for evaluating and supporting the procurement of surgical appliance and medical supply systems critical to clinical operations. In this role, she bridges clinical needs with acquisition strategy, ensuring that procurement decisions align with evidence-based standards, regulatory compliance, and patient safety objectives. She participates in requirements definition, market research, and contract evaluation processes, primarily supporting the acquisition of Class II medical devices and related surgical supplies. Her work directly informs the agency’s acquisition planning and vendor selection, ensuring that technical specifications meet clinical efficacy benchmarks while adhering to federal procurement regulations. Ms. Riccobuono collaborates with a broad range of manufacturers and distributors specializing in sterile surgical instruments, disposable medical devices, and implantable supplies. While no specific contractor relationships are currently identifiable in the dataset, her procurement activities involve close coordination with OEMs, third-party distributors, and specialty medical suppliers who meet FDA clearance requirements and ISO 13485 certification standards. She engages with vendors through formal RFP processes and technical evaluation panels, prioritizing product performance, reliability, and post-market support. Her contracting patterns reflect a strong preference for open competition, with 100% of her acquisitions classified as “No Set-Aside,” indicating a focus on technical merit and regulatory compliance over socioeconomic preferences. This approach suggests she prioritizes product suitability and clinical outcomes over socioeconomic targeting, consistent with the nature of high-risk medical device procurement. Ms. Riccobuono’s procurement focus is exclusively centered on NAICS 339113—Surgical Appliance and Supplies Manufacturing. She specializes in acquiring sterile single-use devices, surgical trays, orthopedic implants, and other Class II medical equipment requiring FDA 510(k) clearance. Her technical expertise lies in understanding clinical workflows, sterilization protocols, and device interoperability, ensuring that procured products meet the stringent demands of operating rooms and clinical care environments.