Top Companies in the Single-Use Consumables Market
- 3M
- Medline Industries
- Cardinal Health
- Becton, Dickinson & Co. (BD)
- Baxter International
- B. Braun Melsungen
- Kimberly-Clark Health / Kimtech
- Ansell
- Terumo Corporation
- Smiths Medical
- ConvaTec
- Coloplast
- Mölnlycke Health Care
- Owens & Minor
- Henry Schein
- Fresenius Kabi
- Teleflex
- Cook Medical
- Nipro Medical
Market Growth
The global single-use consumables market size began at US$ 2.99 billion in 2024 and is forecast to rise to US$ 3.49 billion by 2025. By the end of 2034, it is expected to surpass US$ 13.83 billion, growing steadily at a CAGR of 16.56%.
Single-Use Consumables Market Trends
Adoption of Growth Strategies
Acquisition or partnering with regional players allows large firms to gain immediate market access and distribution networks without starting from scratch. Adoption of growth strategies even assists in accelerating the manufacturing capacity, innovation of new products, and expansion of business.
Investment & Funding
Investment and funding drive the growth of the single-use consumables market by enabling product innovation, scaling manufacturing, and expanding distribution. They support the development of sustainable alternatives, automation, and regulatory compliance. Capital enhances brand differentiation, marketing, and supply chain efficiency. Overall, investment accelerates the production, quality, and reach of consumables, helping companies meet rising global demand across sectors like healthcare, food service, and personal care.
For instance,
- Market Expansion & Vertical Integration for Supply Chain Control
- Market expansion can significantly drive the growth of the single-use consumables market by increasing the demand across various industries and regions.
- In August 2024, Cardinal Health, a pharmaceutical company, revealed its intend to open a distribution center in Walton Hills, Ohio, supporting its U.S. Distribution and Medical Products business.
Market Value Chain Analysis
Research & Development (R&D)
- Innovation in consumables design: Development of advanced disposable bioreactors, tubing sets, filtration units, connectors, and bags optimized for specific bioprocessing needs.
- Material testing: Evaluation of polymers, coatings, and sterilization methods to ensure chemical compatibility, sterility, and durability.
- Process optimization: Integration of single-use systems into upstream and downstream bioprocess workflows for efficiency and scalability.
- Prototyping & pilot studies: Small-scale testing of new consumables with cell cultures or biologics to validate performance.
- Single-use consumables manufacturers – e.g., Sartorius, Thermo Fisher Scientific, GE Healthcare, Merck KGaA
Clinical Trials & Regulatory Approvals
- Clinical trial support: Single-use consumables are used in the production of investigational biologics, vaccines, and cell therapies during Phase I–III studies to ensure sterility and minimize contamination risk.
- Compliance documentation: Manufacturers provide validation data, sterility reports, and biocompatibility testing results to regulatory authorities.
- Regulatory approval process: Consumables must comply with FDA, EMA, or local regulatory standards for GMP, ISO, and quality control to be used in commercial manufacturing.
- Regulatory agencies – FDA (U.S.), EMA (Europe), PMDA (Japan), CDSCO (India) for approvals and compliance. Quality testing labs – third-party labs conducting sterility, biocompatibility, and GMP audits
Formulation & Final Dose Preparation
- Upstream processing: Single-use bioreactors and tubing sets facilitate cell culture, fermentation, or viral vector production.
- Downstream processing: Disposable filtration, chromatography, and purification units are used for product clarification and concentration.
- Final formulation & fill-finish: Bags, connectors, and sterile tubing sets assist in blending, vial filling, lyophilization, and packaging of the final drug product in a contamination-free environment.
- In-house biopharma manufacturing facilities – companies like Pfizer, Moderna, Novartis
Distribution to Hospitals and Pharmacies
- Packaging & labeling: Sterile, pre-assembled consumables are packaged with traceability features.
- Supply chain logistics: Products are transported under controlled conditions to contract manufacturers, hospitals, pharmacies, and specialty clinics.
- Inventory management: Systems like managed inventory or just-in-time delivery ensure seamless availability of consumables for ongoing production and clinical use.
- Pharmaceutical wholesalers and distributors – e.g., McKesson, Cardinal Health, AmerisourceBergen
Patient Support & Services
- Training & technical support: Manufacturers provide guidance to bioprocess operators and hospital staff for correct use of single-use systems.
- Maintenance & replacement services: Timely supply of consumables and replacement parts ensures uninterrupted therapy production and administration.
- After-sales service & documentation: Quality assurance, regulatory compliance support, and troubleshooting for optimized patient outcomes.
- Third-party service providers – companies managing device maintenance, replacement, and compliance documentation
Latest Announcement by Industry Leaders
In May 2025, Lucas Muriello, CFO of USMGC stated that the full-scale opening of the U.S. Medical Glove Company's (USMGC) face mask manufacturing facility is a significant step toward bringing the country's health and safety supply chain back to American territory. With six high-speed lines specifically designed to produce 3-ply disposable face masks, the state-of-the-art facility advances USMGC's dedication to supplying essential medical supplies that are produced in the USA.
Recent Developments in the Single-Use Consumables Market
- In April 2025, INTCO Medical, a leading disposable glove manufacturer has announced the worldwide release of its unique, patented Syntex Synthetic Disposable Latex Gloves. In terms of glove quality, safety, and performance, Syntex is pushing the limits of natural latex. The safety and compliance of Syntex gloves with FDA and EU CE standards are guaranteed by their successful completion of EN455 and EN374 testing dependability in a variety of fields, such as industrial protection, food processing, and healthcare.
- In May 2025, Wadi Surgicals, the leading nitrile glove manufacturer in India, based in Hyderabad, announced the introduction of accelerator-free nitrile gloves under its flagship brand Enliva, marking a significant innovation milestone. These gloves are India's first accelerator-free nitrile gloves, which mark a significant advancement in skin-safe, allergy-free hand protection.
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