Ansys, Inc. is one of 13028 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Ansys, Inc. is an engineering simulation software company with a manufacturing facility in Irvine, California. The company develops computational tools for design and analysis across multiple industries.
Ansys received 1 FDA 510(k) clearance from 1 total submission in the Toxicology device category. The company's cleared device, ON.SITE ALCOHOL, was approved in 1996. Ansys is no longer active in FDA device submissions and should be treated as a historical regulatory record.
Explore the company's device clearance history, product codes, and submission dates in the database.
FDA 510(k) Regulatory Record - Ansys, Inc.
1 devices