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As diversity in types of surgical centers grows, center focus around the cases and trays in which instruments and devices are delivered to the operatory site.
August 8, 2024
By: Mark Crawford
Contributing Editor
Growth is strong in the cases and trays (C&T) orthopedic market, especially in the extremities sector. For example, the overall global procedure trays market size was valued at $17.6 billion in 2022 and expected to expand at a compound annual growth rate of 11.4% from 2023 to 2030. This growth is driven by the increasing number of surgeries, which will “continue to fuel the product demand in the near future,” states Grandview Research.1 Another key driver is increased investment in healthcare infrastructure and “the expansion of medical facilities, such as the rise in surgical centers, worldwide,” said Mike Phillips, president of Phillips Precision Medicraft, an Elmwood Park, N.J.-based manufacturer of custom medical instruments, implant cases, and trays. “These factors contribute to a higher demand for sterilization trays and their components.” Hospitals accounted for over half of the combined global C&T sales in 2022, which reflects their wide variety of needs, including reducing the number of hospital-associated infections through the use of sterile supplies for surgeries and instruments that can be effectively sterilized. “Therefore, doctors and staff in operating rooms are highly dependent on using procedure trays,” stated Grandview Research. “The adoption of procedure trays helps reduce the incidence and operational costs.” The C&T market remains dynamic with constant pricing and timeline pressures. In the rush to get to market, medical device manufacturers (MDMs) tend to overlook case and tray manufacturing, which comes at the final stage, once the instrument designs are frozen. “This puts additional pressure to improve timelines and ensure the synergy of the development teams,” said David Hollner, plant manager for the Rockaway, N.J.-based Intech Group which specializes in contract manufacturing of instruments, cutting tools, implants, silicone handles, cases, and caddies. As critical as the C&T process is for delivering safe and undamaged products, too many MDMs wait until the end of the project to deal with cases and trays, which may result in unwanted delays. Implants and instruments are often fully designed and the project timeline nearly consumed, leaving little time for cases and trays to be developed. Although seemingly straightforward in concept, C&T sets often comprise more than 100 fabricated components, all of which are intensively designed and manufactured. “A deep level of manufacturing expertise and understanding of the tools, instruments, and implants is critical to drive optimal solutions,” said Andrew Thomas, Ph.D., senior director of operations for Indianapolis, Ind.-based Viant Medical, a full-service medical device manufacturer. “Cases and trays cannot be overlooked as a key differentiator for OEMs that want their products to stand out against their competitors and meet evolving customer/patient needs.” Another key role for C&T is aiding compliance with increasingly stringent regulations, such as the new unique device identification (UDI) requirements, which increase tracking and tracing obligations. “These regulations necessitate digital systems and process changes to ensure full traceability throughout the device lifecycle,” said David Ryan, CEO for SMADE, a Lyon, France-based provider of digital tracking solutions for the orthopedic industry. “Implementing UDI requirements can be complex and costly, and is highly dependent on each company’s supply chain model. Additionally, OEMs must rigorously track and prove the efficacy of their devices, ensuring compliance with these stringent regulatory standards.”
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