AG Industries
AG Industries was founded in 1982 as a DME distributor with only 3 employees. As AG began to grow, our specialty quickly became respiratory equipment and the supplies for those systems. As respiratory products became the center of AG, we recognized the constant demand of the systems for disposable supplies, and the red tape that often accompanied their distribution. In order to address those issues AG began to cut, assemble and distribute basic filters to healthcare providers around the country. Along with growing manufacturing capabilities, AG’s innovation grew to include HEPA & custom filters, product design, and a larger focus on fluid filtration including gasses and liquids. Over 37 years, AG has grown to into a vertically integrated company with more than 100 employees and support, with a worldwide presence.
Company details
Find locations served, office locations
- Business Type:
- Manufacturer
- Industry Type:
- Medical / Health Care - Medical Equipment
- Market Focus:
- Globally (various continents)
- Year Founded:
- 1982
- Employees:
- Over 1000
This company also provides solutions for other industrial applications.
Please, visit the following links for more info:
About Us
While manufacturing and supplying a great variety of respiratory products, AG Industries specializes in CPAP, Oxygen Therapy, Suction, Ventilator & Nebulizer filters and replacement accessories. In-house design, engineering and manufacturing ensures AG controls each step of production and delivery of a quality product to customers. When it comes to delivering quality, the well stocked and centrally located facility holds the key to all our client’s aftermarket respiratory needs.
Making a difference with Filtration Group
The Filtration Group family of companies employ more than 6,000 employees in over 100 countries serving a global customer base.
We are committed to making the world safer, healthier and more productive while supporting our local communities.
As a vertically integrated manufacturer and distributor, AG is honored to partner with the members of our distribution chain to provide the best design, parts, products, fulfillment and delivery to our customers and their patients.
Dedicated employees
The AG Industries team is constantly striving to refine our existing products and prepare for future challenges through the integration of research and development within the manufacturing process. By leveraging the skills, expertise, and experience of our dedicated employees we are able to respond quickly to the needs of the industry and form effective relationships with our valued partners.
Breathe easy, change is good
New in 2019, our new Tijuana production facility allows us close-at-hand quality control, cost-competitiveness and a state-of-the art manufacturing environment for even higher purity of product. It’s a smart move, centered on our customers’ needs.
Our Quality Difference
Whether you are seeking to update components of your existing device or create cutting edge, innovative, full filtration systems, we have vertically integrated our manufacturing lines to ensure process and quality control every step of the way. AG will be your partner during concept development, manufacturing, testing, validation, and beyond.
Dedicated to the highest standards of operation through every step of a project, our facilities are FDA registered and are ISO 13485:2016 and MDSAP certified. Over 37 years of experience provides the deep well of resources needed to develop innovative designs and engineering solutions. Additionally, our expert team of engineers, project managers, and quality assurance professionals work with you to ensure a smooth process from the first sparks of creation to submission of your 510(k) applications. Aligning your direction and requirements with our techniques and commitment to excellence is the most efficient and effective path to bring your product to market.
Quality Capabilities
- FDA Registered Facility
- U.S. FDA 510k submissions
- MDD Compliance and CE Marking
- Quality Management System in place
- US 21 CFR 820 Design Control Compliance
- ISO Design Control
- Certified to ISO 13485:2016
- Utilization of ISO 14971 Risk Management Process
- Health Canada Licensed Products
- EU Authorized Representative – Emergo Group
EMERGO EUROPE
Prinsessegracht 20
2514 AP The Hague
The Netherlands
- ISO 13485:2016
- MDSAP Facility
- St. Louis, Missouri
- Tijuana, Mexico