Ecolab, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ecolab, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ecolab POU Water Filter Spray Outlet, Ecolab POU Water Filter Nozzle Outlet, Ecolab POU Water Filter Shower Wand, Ecolab POU Water Filter
Ecolab, Inc. is a global provider of water, hygiene, and infection prevention solutions and services. The company operates with a manufacturing facility in St. Paul, Minnesota, serving diverse industries including healthcare, food and beverage processing, and hospitality.
Ecolab received 7 FDA 510(k) clearances from 7 total submissions between 1988 and 2019. The company's cleared devices span multiple healthcare specialties, including general hospital equipment, gastroenterology and urology devices, and anesthesiology products. The company is currently inactive, with no submissions recorded in the past five years.
Ecolab's FDA-cleared portfolio includes fluid warming drapes, scope pillow warmers, point-of-use water filtration systems, and airway management devices. These products reflect the company's historical focus on perioperative safety, infection control, and water quality in clinical settings.
Explore the complete regulatory record, including device names, product codes, and individual clearance dates in the database.