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Market Size, 2025
$0.88 BnMarket Estimate, 2026
$0.92 BnMarket Forecast, 2034
$1.34 BnCAGR, 2026–2034
4.81%Executive Summary: North America Enteral Feeding Devices Market
- Market Scope: Comprehensive regional industry assessment of the enteral feeding devices market analyzing product types, patient stages, clinical applications, end-use settings, and country-level dynamics.
- Market Valuation: Valued at USD 0.88 billion in 2025, reaching USD 0.92 billion in 2026, and projected to expand to USD 1.34 billion by 2034, registering a steady CAGR of 4.81% from 2026 to 2034.
- Primary Growth Drivers: Rising geriatric populations suffering from neurodegenerative conditions like advanced dementia, increasing cancer prevalence requiring nutritional support, and a higher number of preterm births needing neonatal intensive care management.
Key Market Segment Metrics (2026–2034)
| Category | Leading Segment / Core Focus | Fastest-Growing / Key Segments |
|---|---|---|
| By Product Type | Enteral Feeding Tubes & Pumps (foundational clinical hardware for administering essential liquid nutrition) | Portable / Specialty Feeding Systems (innovative lightweight mobile options like FDA-approved non-electronic mobility devices) |
| By Stage | Adults (dominated by elderly populations managing chronic conditions, dementia, and post-stroke complications) | Pediatrics & Neonates (vital growth segment driven by rising preterm births and critical NICU nutritional management) |
| By Application | Neurological Disorders & Oncology (primary clinical indications causing swallowing difficulties and severe malnutrition) | Gastroenterology & Hyper Metabolism (expanding fields requiring specialized long-term tube placement and metabolic support) |
| By End User | Hospitals (primary healthcare settings handling acute intensive care unit and ventilated patient feeding) | Ambulatory Care Services & Home Care (growing rapidly through supportive home enteral nutrition surveys and programs) |
| By Country | The United States (held the largest market share anchored in advanced healthcare infrastructure and frequent product approvals) | Canada (projected for robust growth driven by home enteral nutrition surveys and favorable reimbursement policies) |
Major Market Players & Market Structure
Market Structure: Consolidated and innovation-driven medical device market dominated by multinational healthcare and medical technology corporations leveraging regulatory approvals and strong hospital distribution networks.
Key Companies: Halyard Health Inc., C. R. Bard Inc., Abbott Laboratories, Fresenius SE, Covidien PLC, Cook Medical, and Nestle S.A.
North America Enteral Feeding Devices Market Size
The North American enteral feeding devices market size was valued at USD 0.88 billion in 2025 and is anticipated to reach USD 0.92 billion in 2026 from USD 1.34 billion by 2034, growing at a CAGR of 4.81% during the forecast period from 2026 to 2034.

Enteral feeding devices represent a crucial medical technology sector dedicated to administering liquid nutrition directly into the gastrointestinal tract of patients suffering from severe intake impairment. According to the Centers for Disease Control and Prevention, over 129000000 individuals in the United States suffer from at least 1 major chronic disease such as cancer, stroke, or severe diabetes that frequently causes gastrointestinal or neurological dysfunction. Enteral feeding systems, encompassing pumps, tubes, and administration sets, are essential for sustaining proper caloric and nutrient intake. As per research published by the American Society for Parenteral and Enteral Nutrition, over 437882 individuals in the United States rely on home enteral nutrition systems to manage chronic nutritional deficits outside acute care environments. The expanding geriatric population across North America significantly amplifies the demand for long term gastrointestinal access lines and automated delivery systems in nursing homes and outpatient residences. Furthermore, as per clinical reports from the Canadian Institute for Health Information, complex care pediatric patients and elderly individuals account for a growing share of specialized medical device management in community care settings. Consequently, North America Enteral Feeding Devices Market development is strongly sustained by rising chronic disease prevalence, expanding home care preferences, and advanced safety standard mandates across clinical settings.
MARKET DRIVERS
Surging Prevalence of Chronic Diseases Propelling Equipment Usage
Growing numbers of patients diagnosed with chronic gastrointestinal and neurological conditions strongly propel the growth of the North American enteral feeding devices market. According to the Centers for Disease Control and Prevention, chronic diseases affect over 129000000 adults in the United States, driving a substantial portion of critical care hospitalizations and prolonged therapies. Enteral delivery equipment provides critical daily nutritional support for patients affected by severe head and neck cancers, acute strokes, and neurodegenerative disorders that impair normal swallowing functions. As per the National Center for Health Statistics, over 39.8% of senior men and 28.6% of senior women aged 85 and older live with diagnosed cancer conditions that frequently mandate clinical enteral intervention. The direct correlation between chronic illness hospitalizations and enteral intake management drives high volume consumption of enteral pumps, nasoenteric lines, and specialized administration sets across clinical facilities. In addition, extended survival rates among cancer patients treated with aggressive chemotherapy or radiotherapy create continuous demand for temporary nasogastric access lines and permanent gastrostomy tubes during therapeutic rehabilitation cycles. Rising oncological treatment protocols in regional hospitals mandate continuous purchases of high precision fluid delivery systems to minimize severe patient weight loss and therapeutic malnutrition.
Expanding Home Parenteral and Enteral Support Boosting Demand
Accelerated shifts toward outpatient management and home healthcare services strongly boost the North American enteral feeding devices market expansion. According to the American Society for Parenteral and Enteral Nutrition, approximately 437882 total patients across the United States rely on home enteral tube feeding therapies to maintain daily nutritional health. Transitioning post acute patients from intensive clinical care to residential settings requires portable feeding pumps, user friendly administration sets, and durable gastrostomy tubes designed for non professional caregivers. As per findings published in the Journal of Parenteral and Enteral Nutrition, over 248846 adult patients and 189036 pediatric patients actively receive home enteral nutrition in domestic residential care programs. The ongoing expansion of home care network models ensures a continuous demand for portable, highly automated, and fail safe enteral delivery equipment across North America. Regional home healthcare agencies actively partner with medical device manufacturers to integrate telehealth capabilities and remote monitoring software into home infusion systems. This structural shift away from expensive prolonged inpatient stays allows patients to recover safely at home, driving stable, high volume retail and institutional sales for specialized ambulatory feeding pumps and reusable gravity feeding kits.
MARKET RESTRAINTS
Severe Complications and Mechanical Misconnections Restricting Market Adoption
High risk occurrences of clinical tube misconnections and gastrointestinal complications severely restrict the market expansion of conventional enteral delivery hardware. According to the United States Food and Drug Administration, accidental enteral misconnections linking feeding sets to intravenous lines or epidural catheters have resulted in severe patient injury and fatal outcomes across clinical facilities. Inserting gastrostomy and nasoenteric tubes presents inherent clinical risks including aspiration pneumonia, tube dislodgement, localized mucosal ulceration, and severe insertion site infections. As per clinical safety data published in the Journal of Patient Safety, misconnections involving medical tubing represent persistent adverse health events that force healthcare institutions to conduct costly risk mitigation protocols. These persistent medical risks, paired with substantial liability concerns for healthcare providers, create caution among clinicians and hamper broader product adoption rates across non tertiary healthcare facilities. Frequent emergency room readmissions caused by clogged or displaced feeding tubes increase total healthcare expenditure, leading risk adverse medical groups to explore alternative feeding pathways when possible. Furthermore, strict institutional reporting rules regarding adverse medical device events force clinical centers to spend extensive resources on staff retraining, delaying the rapid procurement of non-standard tubing designs.
High Initial Capital Outlays and Maintenance Costs Hindering Outpatient Growth
Elevated equipment procurement expenses and ongoing maintenance overheads significantly hinder market growth across budget constrained home care agencies. According to the Emergency Research Institute, high technology smart enteral pumps equipped with dose error reduction systems carry high initial purchase costs compared to traditional gravity administration sets. Acquiring electronic pumps, specialized compatible sets, and replacement lines places financial pressure on outpatient care providers operating under fixed reimbursement models. As per medical expenditure analysis from the Agency for Healthcare Research and Quality, high device costs combined with capitated insurance coverage limit the rapid deployment of advanced electronic delivery systems in home settings. These financial hurdles restrict small home healthcare providers from acquiring automated equipment, delaying broader device market penetration across rural healthcare regions. Financial constraints are exacerbated by fluctuating insurance reimbursement rates for specialized disposable accessories, forcing healthcare providers to reuse low cost administration sets or delay system upgrades. Capital equipment budget freezes in smaller community hospitals further prevent the widespread replacement of aging volumetric pumps, creating a distinct commercial barrier for innovative high cost digital platforms.
MARKET OPPORTUNITIES
Widespread ENFit ISO Standard Transitions Offering Product Upgrade Avenues
The industry wide transition toward ENFit standardized small bore connectors creates an commercial opportunity for medical equipment manufacturers upgrading North American inventories. According to the Global Enteral Device Supplier Association, adopting ISO 80369 3 safety standard connectors eliminates tube misconnection risks by preventing compatibility with non enteral fluid lines. Medical facilities and home care providers across North America are systematically replacing legacy tubing systems with ENFit compliant pumps, syringes, gravity sets, and enteral access lines. As per clinical evaluation studies published in Hospital Pharmacy, transitioning to ENFit safety compliant connectors significantly reduces cross connection incidents, prompting comprehensive inventory turnovers across acute care hospital systems. Manufacturers engineering proprietary, low dose tip ENFit syringes and specialized adapter sets can secure lucrative long term supply contracts across major North American healthcare networks. Federal regulatory pressure to mandate standardized enteral locking mechanisms compels clinical procurement managers to replace legacy hardware across intensive care units and long term nursing facilities. This mandatory equipment turnover opens up significant market expansion avenues for agile device producers capable of manufacturing high volume, fully compliant ENFit connector assemblies.
Automated Smart Pump Integration Creating Advanced Technological Avenues
Integrating digital software platforms and smart monitoring features into modern enteral feeding pumps offers a lucrative opportunity for advanced technology developers in the North American enteral feeding devices market. According to the American Society for Health System Pharmacists, implementing smart infusion technology with dose error reduction systems reduces medication and formula administration errors in critical care units by over 70%. Modern smart pumps feature custom programmable flow rates, wireless electronic health record data synchronization, and automated occlusion alarm systems that optimize patient monitoring efficiency. As per clinical telemetry reports from the Healthcare Information and Management Systems Society, digital health integrations in intensive care units streamline nursing workflows and improve clinical documentation accuracy. Developing user friendly, mobile app linked enteral pumps enables medical device firms to capture high margin replacement contracts in both hospital and home healthcare sectors. Advanced software algorithms that allow remote clinicians to adjust formula administration rates in real time transform patient monitoring capabilities in outpatient settings. Building integrated digital healthcare ecosystems provides device manufacturers with recurring software subscription revenues while improving therapeutic precision and lowering clinical workload across major North American hospital networks.
MARKET CHALLENGES
Stringent FDA Regulatory Oversight Challenging Product Approval Timelines
Intensive regulatory requirements enforced by federal health agencies create severe technological barriers that challenge product development pipelines for new market entrants. According to the United States Food and Drug Administration, enteral feeding pumps and modified enteral tubes are classified as Class II medical devices requiring rigorous 510k premarket notification clearances, human factors testing, and design validation trials. Submitting comprehensive safety documentation regarding biocompatibility, mechanical durability, and software reliability requires substantial financial investment and extends commercial development timelines. As per regulatory review metrics published by the Regulatory Affairs Professionals Society, medical device clearance timelines can exceed 12 months for complex digital infusion technologies. Small scale device developers face high capital consumption while attempting to clear stringent regulatory hurdles, limiting new product introductions and compressing profit margins across North American operations. Heightened federal scrutiny regarding cybersecurity protocols in wireless smart pumps adds extensive validation steps to the software engineering cycle. Consequently, small medical engineering firms often struggle to maintain liquidity while navigating multi year clinical testing mandates, leaving market dominance restricted to large multinational health technology enterprises.
Volatile Raw Material Costs and Supply Chain Vulnerabilities Challenging Production
Persistent supply chain disruptions and shifting raw polymer material expenses challenge the North American enteral feeding devices market expansion. According to the Association for Health Care Resource and Materials Management, healthcare supply chains in North America experienced average medical supply price inflation exceeding 6.5% during recent operational periods, directly elevating component manufacturing costs. Disposable enteral feeding sets require medical grade polyvinyl chloride, polyurethane, and silicone to ensure biocompatibility and flexibility during prolonged fluid transmission. As per industry logistics reports from the Health Manufacturers Association, disruptions in global raw resin refining and transportation networks create critical component shortages for tube manufacturers. Additive regulatory restrictions on phthalates in medical grade polymers force compounders to source specialized bio based alternatives, raising manufacturing costs and creating production bottlenecks for disposable line producers. Fluctuating transportation expenses and overseas raw material delays frequently interrupt automated manufacturing schedules for disposable feeding sets and fluid reservoirs. Plastic resin price surges force manufacturers to either absorb narrowed operational margins or attempt to pass cost increases along to price sensitive hospital purchasing alliances.
REPORT COVERAGE
| REPORT METRIC | DETAILS |
| Market Size Available | 2025 to 2034 |
| Base Year | 2025 |
| Forecast Period | 2026 to 2034 |
| CAGR | 4.81% |
| Segments Covered | By Product Type, Stage, Application, End-Use and Region |
| Various Analyses Covered | Global, Regional & Country Level Analysis, Segment-Level Analysis; DROC; PESTLE Analysis; Porter’s Five Forces Analysis, Competitive Landscape; Analyst Overview of Investment Opportunities |
| Regions Covered | The United States, Canada, Rest of North America |
| Market Leaders Profiled | Halyard Health Inc., C. R. Bard Inc., Abbott Laboratories, Fresenius SE, Covidien PLC, Cook Medical, and Nestle S.A. |
SEGMENTAL ANALYSIS
By Product Type Insights
The enteral feeding tubes segment accounted for the major share of the North American enteral feeding devices market in 2025 because they are mandatory for direct gastrointestinal access across both short term and long term patient care regimes. Enteral feeding tubes, including nasoenteric, oroenteric, and enterostomy variations, are required for every enteral administration procedure regardless of whether fluids are delivered via pumps or gravity bags. According to the Centers for Disease Control and Prevention, over 129000000 American adults suffer from chronic illnesses that frequently necessitate long term nutritional support via gastrostomy or jejunostomy surgical tube placements. Furthermore, as per the American Society for Parenteral and Enteral Nutrition, over 437882 individuals in the United States currently depend on home tube feeding, driving perpetual volume replacement demand for gastrostomy tubes and nasogastric access lines. The absolute operational necessity of access tubes across all clinical enteral protocols secures their position as the leading revenue segment. Medical practitioners continuously rely on enteral tubes for administering specialized formulas, oral medications, and rehydration fluids to critically ill patients across all care tiers. The recurring nature of tube replacements, caused by normal mechanical wear or scheduled clinical rotations, generates continuous revenue streams for tubing manufacturers. Expanding surgical placements of percutaneous endoscopic gastrostomy tubes among chronic neurological patients further cements this product category as the structural backbone of the broader device industry.
On the other end, the enteral feeding pumps segment is predicted to register a CAGR of 7.2% over te forecast period in the regional market owing to the rapid adoption of automated flow control and smart safety technologies across North America. Enteral feeding pumps deliver precise, continuous, or intermittent nutrient volumes, which significantly reduces the risk of gastrointestinal intolerance and aspiration complications in critically ill patients. According to the American Society for Health System Pharmacists, smart pumps equipped with dose error reduction systems cut formula administration errors by over 70% in hospital critical care settings, accelerating their mandatory adoption in acute units. Furthermore, as per the American Society for Parenteral and Enteral Nutrition, 248846 adult home care patients require portable, battery operated electronic pumps to manage daily feeding regimens independently. Rising home care preferences and digital health record integrations continue to drive rapid market expansion for programmable smart pumps. Modern digital pumps feature compact designs, extended battery life, and customizable flushing sequences that significantly improve patient mobility in residential settings. The market transition toward automated, failure proof fluid management systems encourages healthcare systems to replace legacy manual gravity sets with digital volumetric pumps across all major clinical departments.
By Stage Insights
The adult stage segment led the market by capturing the highest share of the North American market in 2025 due to the high incidence of chronic diseases, age related dysphagia, and acute trauma in mature populations. Aging demographic shifts significantly expand the patient pool requiring short term and permanent enteral feeding support in hospitals and long term care facilities. According to the National Center for Health Statistics, over 66.9% of U.S. adults aged 85 and older live with hypertension, 39.8% of senior men have cancer, and 31.5% suffer from heart disease, conditions that frequently require clinical nutritional interventions. Furthermore, as per data from the American Society for Parenteral and Enteral Nutrition, adult home enteral nutrition users number 248846 individuals, vastly outnumbering pediatric patient cohorts. The combination of widespread chronic illness and extended lifespans reinforces the clear dominance of the adult patient segment. High clinical rates of stroke, head and neck trauma, and progressive neurodegenerative conditions such as Parkinson's disease among mature adults drive persistent demands for gastrostomy tube placements. Long term care facilities and nursing homes maintain continuous purchasing agreements for adult size administration sets, gravity bags, and electronic pumps to manage daily resident care. As the regional population continues to age, adult clinical nutrition management remains the primary revenue driver for medical device distributors.
However, the pediatric segment is the fastest growing stage category and is expected to progress at a CAGR of 6.5% over the forecast period owing to the increased survival rates among premature infants and heightened awareness of pediatric congenital disorders. Neonatal intensive care units rely heavily on specialized micro bore enteral tubes and precision low volume pumps to sustain low birth weight infants. According to the National Center for Health Statistics, pre term birth rates in the United States affect approximately 10.4% of all live births, creating an immediate demand for specialized neonatal enteral delivery devices. Furthermore, as per research published by the American Society for Parenteral and Enteral Nutrition, there are currently 189036 pediatric patients receiving home enteral nutrition therapies across domestic residential settings. Growing clinical emphasis on early pediatric nutritional interventions to prevent long term developmental deficits drives high growth for specialized pediatric enteral hardware. Specialized pediatric feeding devices require soft, highly flexible, bio-compatible materials and ultra-low dose tip connectors to protect delicate infant gastrointestinal tracts. Expanding specialized pediatric home care networks across North America allow families to manage long term congenital swallowing disorders outside hospital environments safely. High clinical investments in specialized neonatal intensive care technology ensure that pediatric enteral equipment maintains rapid market growth across regional children's healthcare facilities.
COUNTRY ANALYSIS
U.S. Enteral Feeding Devices Market Analysis
The U.S. dominated the market by commanding 85.7% of the North American market share in 2025 and is functioning as the central hub for advanced clinical technology adoption and medical equipment manufacturing. Extremely high chronic disease prevalence across an aging population drives massive operational demand for automated enteral pumps, ENFit compatible administration sets, and gastrostomy tubes. According to the Centers for Disease Control and Prevention, over 129000000 American adults live with at least 1 chronic health condition, creating a vast baseline requirement for long term clinical and outpatient nutritional support. As per the American Society for Parenteral and Enteral Nutrition, over 437882 individuals in the United States actively utilize home enteral feeding devices to manage chronic nutritional deficits outside acute care institutions. Favorable Medicare and private health insurance reimbursement coverage for home enteral nutrition supplies further accelerates continuous equipment adoption across outpatient networks. Widespread integration of electronic health records and smart hospital technologies reinforces the demand for connected smart enteral pumps in intensive care environments. Domestic manufacturers maintain aggressive research pipelines to expand low dose tip ENFit safety portfolios, ensuring the United States maintains its dominant position across North American clinical and home healthcare markets. Extensive group purchasing organization networks streamline device distribution to thousands of acute hospitals and nursing homes nationwide, maintaining high baseline hardware utilization rates. Capital investments by major U.S. health systems in smart infusion pump platforms continue to push commercial demand for next generation digital enteral delivery hardware.
Canada Enteral Feeding Devices Market Analysis
Canada represents an emerging and highly stable market segment and is supported by a publicly funded healthcare system. Government health programs prioritize cost effective outpatient management, driving steady adoption of home enteral nutrition equipment and long term care feeding solutions. According to the Canadian Institute for Health Information, provincial healthcare systems manage over 250000 annual hospital admissions related to gastrointestinal, neurological, and surgical conditions requiring enteral nutritional support. As per Statistics Canada, over 19.0% of the Canadian population is aged 65 and older, accelerating chronic disease diagnoses and expanding demand for specialized enterostomy access lines. Provincial health authorities actively enforce ISO safety mandates, accelerating the systemic replacement of legacy medical tubing with ENFit compliant connectors across acute care facilities. Strong institutional focus on reducing acute hospital bed occupancy drives expanding government funding for home enteral care supplies and portable infusion pumps. Canadian healthcare facilities continuously partner with global device distributors to ensure a secure supply of biocompatible, non-phthalate enteral administration lines. This structural shift toward home care delivery paired with universal healthcare reimbursement models supports consistent, reliable market growth across all Canadian provinces. Expanding provincial funding for long term community care programs ensures stable demand for durable gastrostomy hardware and portable pumps in residential settings. Canadian medical centers remain active adopters of standardized tubing safety designs, creating a predictable market for international device suppliers.
COMPETITIVE LANDSCAPE
The competitive landscape of the North America Enteral Feeding Devices Market is highly consolidated, dominated by a small group of multinational medical technology corporations alongside specialized gastrointestinal device developers. Key competitors engage in intense rivalry based on product safety features, smart software integration, pricing, and distribution network reach. Strict regulatory requirements enforced by federal health authorities create exceptionally high entry barriers for new competitors, as clearing 510k device applications requires comprehensive biocompatibility testing and clinical human factors validation. Competition is further heightened by the industry wide shift toward ENFit standardized connectors, forcing non compliant suppliers out of major hospital networks. Established market leaders maintain strong competitive advantages through long term supply contracts with group purchasing organizations and integrated clinical nutrition service offerings across both acute hospital environments and expanding home care sectors.
KEY MARKET PLAYERS
Companies playing a dominant role in the North American Enteral Feeding Devices Market include
- Halyard Health Inc.
- C. R. Bard Inc.
- Abbott Laboratories
- Fresenius SE.
- Covidien PLC
- Cook Medical
- Nestle S.A.
Top Players Contribution
Cardinal Health Inc. Insights
Cardinal Health Inc. contributes significantly to the enteral market through its extensive Kangaroo portfolio of enteral feeding pumps, administration sets, and ENFit safety accessories. The company focuses on enhancing patient safety by providing automated dose error reduction software and low dose tip tubing connectors designed to eliminate medical misconnection incidents. To strengthen its market leadership, Cardinal Health Inc. expanded its medical supply manufacturing and distribution infrastructure in early 2023, increasing production capacity for Kangaroo OMNI smart enteral pumps across North American healthcare networks.
Avanos Medical Inc
Avanos Medical Inc. provides vital market contributions through its widely recognized MIC KEY and MIC line of enteral feeding tubes and gastrostomy access systems. The company specializes in low profile, balloon retained enteral access hardware engineered to improve patient comfort in both pediatric and adult home care settings. To reinforce its competitive market standing, Avanos Medical Inc. acquired Trident Medical Devices in October 2022, acquiring advanced manufacturing capabilities for gastrointestinal access lines and expanding its specialized ENFit safety product lines across hospital networks.
Fresenius Kabi AG
Fresenius Kabi AG contributes extensively to the regional market by offering integrated clinical nutrition solutions, including the Amika enteral feeding pump series and specialized delivery sets. The firm prioritizes total clinical nutrition care by combining enteral hardware with customized liquid formula lines for intensive care units. To solidify its market presence in North America, Fresenius Kabi AG completed a major expansion of its North Carolina manufacturing and packaging facility in September 2023, significantly boosting domestic production of ENFit compatible enteral delivery sets and pump accessories.
Top Strategies Used by Key Market Participants
Key participants in the North America Enteral Feeding Devices Market prioritize strategic portfolio safety upgrades, digital healthcare integrations, and targeted corporate acquisitions to secure long term market growth. Leading manufacturers allocate substantial capital toward engineering ISO 80369 3 compliant ENFit connectors across all tubing portfolios to eliminate misconnection hazards and satisfy strict clinical safety mandates. Companies actively integrate wireless connectivity and custom dose error reduction software into electronic smart pumps to allow automated patient data transfer to hospital electronic health record systems. Strategic partnerships with home healthcare agencies, regional medical equipment distributors, and major hospital buying networks ensure consistent supply distribution. Furthermore, key players execute strategic brownfield facility expansions and tactical acquisitions of specialized tube developers to secure raw material supplies, broaden proprietary product lines, and protect market share against foreign competitors.
RECENT MARKET DEVELOPMENTS
- In October 2022, Avanos Medical Inc., a leading medical technology provider, acquired Trident Medical Devices, a specialized gastrointestinal access company. This acquisition is anticipated to allow Avanos Medical Inc. to offer more comprehensive enteral access solutions and strengthen the North America Enteral Feeding Devices Market.
- In January 2023, Cardinal Health Inc., a major healthcare service provider, expanded its Kangaroo enteral feeding product portfolio by launching the Kangaroo OMNI enteral feeding pump. This product launch is anticipated to allow Cardinal Health Inc. to offer more versatile portable feeding solutions and strengthen the North America Enteral Feeding Devices Market.
- In September 2023, Fresenius Kabi AG, a global healthcare firm, completed a major expansion of its North American manufacturing plant in North Carolina. This expansion is anticipated to allow Fresenius Kabi AG to offer higher volumes of ENFit compatible administration sets and strengthen the North America Enteral Feeding Devices Market.
- In November 2023, Moog Inc., an advanced motion control developer, launched its updated Enterprise smart enteral pump software platform. This software release is anticipated to allow Moog Inc. to offer superior wireless electronic health record integration and strengthen the North America Enteral Feeding Devices Market.
- In March 2024, B. Braun Melsungen AG, a medical device producer, expanded its Enteroport plus enteral pump distribution network across North American healthcare facilities. This distribution deal is anticipated to allow B. Braun Melsungen AG to offer broader ambulatory nutrition options and strengthen the North America Enteral Feeding Devices Market.
MARKET SEGMENTATION
This research report on the North American enteral feeding devices market has been segmented and sub-segmented into the following categories.
By Product Type
- Enteral Feeding Tubes
- Nasoenteric Feeding Tubes
- Oroenteric Feeding Tubes
- Enterostomy Tubes
- Enteral Feeding Pumps
- Giving Sets
- Administration Reservoirs
- Enteral Syringes
- Others
By Stage
- Adults
- Pediatrics
By Application
- Gastroenterology
- Neurological Disorders
- Oncology
- Diabetes
- Hyper Metabolism
By End User
- Ambulatory Care Services
- Hospitals
- Others
By Country
- The United States
- Canada
- Rest of North America