Praxair, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Praxair, Inc. - FDA 510(k) Cleared Devices
Recent clearances: The NOxBOXi Nitric Oxide Delivery System
2
Total
2
Cleared
0
Denied
Praxair, Inc. is a leading global industrial gases and engineering company with a manufacturing facility in Tonawanda, US. The company specializes in gas supply systems and related technologies across multiple industrial sectors.
Praxair has received 2 FDA 510(k) clearances from 2 total submissions. The company's regulatory focus is entirely concentrated on Anesthesiology devices, with clearances spanning from 2005 to 2020. This represents a historical record of FDA regulatory activity; the company has not received clearances in more than five years.
Praxair's cleared Anesthesiology devices include specialized gas delivery and mixing systems designed for clinical anesthesia applications. These products reflect the company's expertise in precision gas handling and medical gas system engineering.
For detailed information on device names, product codes, and clearance dates, explore the full regulatory record in the 510(k) database.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Praxair, Inc.
2 devices